Name: rs10605521
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs10605521

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:99143134-99143159 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / d…
del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: delTTT=0.1049 (718/6846, ALFA)
delTTT=0.030 (18/598, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TSGA10 : Intron Variant
C2orf15 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6846	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.8894	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.1049, TTTTTTTTTTTTTTTTTTTTTTTT=0.0057, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.799645	0.010343	0.190012	0
European	Sub	5826	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.8706	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.1227, TTTTTTTTTTTTTTTTTTTTTTTT=0.0067, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.765136	0.012178	0.222686	2
African	Sub	722	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	36	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	686	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	30	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	142	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	94	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.97	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.93617	0.0	0.06383	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6846	(T)₂₆=0.8894	del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.1049, delTT=0.0057, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	5826	(T)₂₆=0.8706	del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.1227, delTT=0.0067, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	722	(T)₂₆=1.000	del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	142	(T)₂₆=1.000	del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	94	(T)₂₆=0.97	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.03, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	30	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	14	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Northern Sweden	ACPOP	Study-wide	598	(T)₂₆=0.970	delTTT=0.030

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 2	NC_000002.12:g.99143145_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143146_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143147_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143148_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143149_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143150_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143151_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143153_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143154_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143155_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143156_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143157_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143158_99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143159del
GRCh38.p14 chr 2	NC_000002.12:g.99143159dup
GRCh38.p14 chr 2	NC_000002.12:g.99143158_99143159dup
GRCh38.p14 chr 2	NC_000002.12:g.99143157_99143159dup
GRCh38.p14 chr 2	NC_000002.12:g.99143156_99143159dup
GRCh38.p14 chr 2	NC_000002.12:g.99143155_99143159dup
GRCh38.p14 chr 2	NC_000002.12:g.99143154_99143159dup
GRCh37.p13 chr 2	NC_000002.11:g.99759608_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759609_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759610_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759611_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759612_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759613_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759614_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759616_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759617_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759618_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759619_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759620_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759621_99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759622del
GRCh37.p13 chr 2	NC_000002.11:g.99759622dup
GRCh37.p13 chr 2	NC_000002.11:g.99759621_99759622dup
GRCh37.p13 chr 2	NC_000002.11:g.99759620_99759622dup
GRCh37.p13 chr 2	NC_000002.11:g.99759619_99759622dup
GRCh37.p13 chr 2	NC_000002.11:g.99759618_99759622dup
GRCh37.p13 chr 2	NC_000002.11:g.99759617_99759622dup

Gene: C2orf15, chromosome 2 open reading frame 15 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C2orf15 transcript variant 1	NM_001317992.2:c.-265+744… NM_001317992.2:c.-265+744_-265+758del	N/A	Intron Variant
C2orf15 transcript variant 2	NM_144706.4:c.-169+744_-1… NM_144706.4:c.-169+744_-169+758del	N/A	Intron Variant

Gene: TSGA10, testis specific 10 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TSGA10 transcript variant 4	NM_001349013.2:c.-519+115… NM_001349013.2:c.-519+11545_-519+11559del	N/A	Intron Variant
TSGA10 transcript variant 1	NM_025244.4:c.-621+11545_… NM_025244.4:c.-621+11545_-621+11559del	N/A	Intron Variant
TSGA10 transcript variant 3	NM_001349012.1:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant 5	NM_001349014.1:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant 2	NM_182911.4:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant 6	NR_146001.2:n.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant 7	NR_146053.2:n.	N/A	Genic Downstream Transcript Variant
TSGA10 transcript variant 8	NR_146054.1:n.	N/A	Genic Downstream Transcript Variant
TSGA10 transcript variant 9	NR_146055.2:n.	N/A	Genic Downstream Transcript Variant
TSGA10 transcript variant X11	XM_017005041.3:c.-529+115… XM_017005041.3:c.-529+11545_-529+11559del	N/A	Intron Variant
TSGA10 transcript variant X3	XM_047445928.1:c.33+11143… XM_047445928.1:c.33+11143_33+11157del	N/A	Intron Variant
TSGA10 transcript variant X4	XM_047445929.1:c.33+11143… XM_047445929.1:c.33+11143_33+11157del	N/A	Intron Variant
TSGA10 transcript variant X5	XM_047445930.1:c.33+11143… XM_047445930.1:c.33+11143_33+11157del	N/A	Intron Variant
TSGA10 transcript variant X6	XM_047445931.1:c.33+11143… XM_047445931.1:c.33+11143_33+11157del	N/A	Intron Variant
TSGA10 transcript variant X7	XM_047445932.1:c.33+11143… XM_047445932.1:c.33+11143_33+11157del	N/A	Intron Variant
TSGA10 transcript variant X16	XM_047445934.1:c.-400+116… XM_047445934.1:c.-400+11689_-400+11703del	N/A	Intron Variant
TSGA10 transcript variant X10	XM_005264023.2:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X15	XM_006712781.3:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X1	XM_011511934.1:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X8	XM_011511935.4:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X2	XM_017005035.2:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X9	XM_017005037.1:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X13	XM_017005044.2:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X17	XM_017005046.2:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X14	XM_024453158.2:c.	N/A	Genic Upstream Transcript Variant
TSGA10 transcript variant X12	XM_047445933.1:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₆=	del(T)₁₅	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆
GRCh38.p14 chr 2	NC_000002.12:g.99143134_99143159=	NC_000002.12:g.99143145_99143159del	NC_000002.12:g.99143146_99143159del	NC_000002.12:g.99143147_99143159del	NC_000002.12:g.99143148_99143159del	NC_000002.12:g.99143149_99143159del	NC_000002.12:g.99143150_99143159del	NC_000002.12:g.99143151_99143159del	NC_000002.12:g.99143153_99143159del	NC_000002.12:g.99143154_99143159del	NC_000002.12:g.99143155_99143159del	NC_000002.12:g.99143156_99143159del	NC_000002.12:g.99143157_99143159del	NC_000002.12:g.99143158_99143159del	NC_000002.12:g.99143159del	NC_000002.12:g.99143159dup	NC_000002.12:g.99143158_99143159dup	NC_000002.12:g.99143157_99143159dup	NC_000002.12:g.99143156_99143159dup	NC_000002.12:g.99143155_99143159dup	NC_000002.12:g.99143154_99143159dup
GRCh37.p13 chr 2	NC_000002.11:g.99759597_99759622=	NC_000002.11:g.99759608_99759622del	NC_000002.11:g.99759609_99759622del	NC_000002.11:g.99759610_99759622del	NC_000002.11:g.99759611_99759622del	NC_000002.11:g.99759612_99759622del	NC_000002.11:g.99759613_99759622del	NC_000002.11:g.99759614_99759622del	NC_000002.11:g.99759616_99759622del	NC_000002.11:g.99759617_99759622del	NC_000002.11:g.99759618_99759622del	NC_000002.11:g.99759619_99759622del	NC_000002.11:g.99759620_99759622del	NC_000002.11:g.99759621_99759622del	NC_000002.11:g.99759622del	NC_000002.11:g.99759622dup	NC_000002.11:g.99759621_99759622dup	NC_000002.11:g.99759620_99759622dup	NC_000002.11:g.99759619_99759622dup	NC_000002.11:g.99759618_99759622dup	NC_000002.11:g.99759617_99759622dup
C2orf15 transcript variant 1	NM_001317992.2:c.-265+733=	NM_001317992.2:c.-265+744_-265+758del	NM_001317992.2:c.-265+745_-265+758del	NM_001317992.2:c.-265+746_-265+758del	NM_001317992.2:c.-265+747_-265+758del	NM_001317992.2:c.-265+748_-265+758del	NM_001317992.2:c.-265+749_-265+758del	NM_001317992.2:c.-265+750_-265+758del	NM_001317992.2:c.-265+752_-265+758del	NM_001317992.2:c.-265+753_-265+758del	NM_001317992.2:c.-265+754_-265+758del	NM_001317992.2:c.-265+755_-265+758del	NM_001317992.2:c.-265+756_-265+758del	NM_001317992.2:c.-265+757_-265+758del	NM_001317992.2:c.-265+758del	NM_001317992.2:c.-265+758dup	NM_001317992.2:c.-265+757_-265+758dup	NM_001317992.2:c.-265+756_-265+758dup	NM_001317992.2:c.-265+755_-265+758dup	NM_001317992.2:c.-265+754_-265+758dup	NM_001317992.2:c.-265+753_-265+758dup
TSGA10 transcript variant 4	NM_001349013.2:c.-519+11559=	NM_001349013.2:c.-519+11545_-519+11559del	NM_001349013.2:c.-519+11546_-519+11559del	NM_001349013.2:c.-519+11547_-519+11559del	NM_001349013.2:c.-519+11548_-519+11559del	NM_001349013.2:c.-519+11549_-519+11559del	NM_001349013.2:c.-519+11550_-519+11559del	NM_001349013.2:c.-519+11551_-519+11559del	NM_001349013.2:c.-519+11553_-519+11559del	NM_001349013.2:c.-519+11554_-519+11559del	NM_001349013.2:c.-519+11555_-519+11559del	NM_001349013.2:c.-519+11556_-519+11559del	NM_001349013.2:c.-519+11557_-519+11559del	NM_001349013.2:c.-519+11558_-519+11559del	NM_001349013.2:c.-519+11559del	NM_001349013.2:c.-519+11559dup	NM_001349013.2:c.-519+11558_-519+11559dup	NM_001349013.2:c.-519+11557_-519+11559dup	NM_001349013.2:c.-519+11556_-519+11559dup	NM_001349013.2:c.-519+11555_-519+11559dup	NM_001349013.2:c.-519+11554_-519+11559dup
TSGA10 transcript variant 1	NM_025244.2:c.-621+11559=	NM_025244.2:c.-621+11545_-621+11559del	NM_025244.2:c.-621+11546_-621+11559del	NM_025244.2:c.-621+11547_-621+11559del	NM_025244.2:c.-621+11548_-621+11559del	NM_025244.2:c.-621+11549_-621+11559del	NM_025244.2:c.-621+11550_-621+11559del	NM_025244.2:c.-621+11551_-621+11559del	NM_025244.2:c.-621+11553_-621+11559del	NM_025244.2:c.-621+11554_-621+11559del	NM_025244.2:c.-621+11555_-621+11559del	NM_025244.2:c.-621+11556_-621+11559del	NM_025244.2:c.-621+11557_-621+11559del	NM_025244.2:c.-621+11558_-621+11559del	NM_025244.2:c.-621+11559del	NM_025244.2:c.-621+11559dup	NM_025244.2:c.-621+11558_-621+11559dup	NM_025244.2:c.-621+11557_-621+11559dup	NM_025244.2:c.-621+11556_-621+11559dup	NM_025244.2:c.-621+11555_-621+11559dup	NM_025244.2:c.-621+11554_-621+11559dup
TSGA10 transcript variant 1	NM_025244.4:c.-621+11559=	NM_025244.4:c.-621+11545_-621+11559del	NM_025244.4:c.-621+11546_-621+11559del	NM_025244.4:c.-621+11547_-621+11559del	NM_025244.4:c.-621+11548_-621+11559del	NM_025244.4:c.-621+11549_-621+11559del	NM_025244.4:c.-621+11550_-621+11559del	NM_025244.4:c.-621+11551_-621+11559del	NM_025244.4:c.-621+11553_-621+11559del	NM_025244.4:c.-621+11554_-621+11559del	NM_025244.4:c.-621+11555_-621+11559del	NM_025244.4:c.-621+11556_-621+11559del	NM_025244.4:c.-621+11557_-621+11559del	NM_025244.4:c.-621+11558_-621+11559del	NM_025244.4:c.-621+11559del	NM_025244.4:c.-621+11559dup	NM_025244.4:c.-621+11558_-621+11559dup	NM_025244.4:c.-621+11557_-621+11559dup	NM_025244.4:c.-621+11556_-621+11559dup	NM_025244.4:c.-621+11555_-621+11559dup	NM_025244.4:c.-621+11554_-621+11559dup
C2orf15 transcript	NM_144706.2:c.-67+733=	NM_144706.2:c.-67+744_-67+758del	NM_144706.2:c.-67+745_-67+758del	NM_144706.2:c.-67+746_-67+758del	NM_144706.2:c.-67+747_-67+758del	NM_144706.2:c.-67+748_-67+758del	NM_144706.2:c.-67+749_-67+758del	NM_144706.2:c.-67+750_-67+758del	NM_144706.2:c.-67+752_-67+758del	NM_144706.2:c.-67+753_-67+758del	NM_144706.2:c.-67+754_-67+758del	NM_144706.2:c.-67+755_-67+758del	NM_144706.2:c.-67+756_-67+758del	NM_144706.2:c.-67+757_-67+758del	NM_144706.2:c.-67+758del	NM_144706.2:c.-67+758dup	NM_144706.2:c.-67+757_-67+758dup	NM_144706.2:c.-67+756_-67+758dup	NM_144706.2:c.-67+755_-67+758dup	NM_144706.2:c.-67+754_-67+758dup	NM_144706.2:c.-67+753_-67+758dup
C2orf15 transcript variant 2	NM_144706.4:c.-169+733=	NM_144706.4:c.-169+744_-169+758del	NM_144706.4:c.-169+745_-169+758del	NM_144706.4:c.-169+746_-169+758del	NM_144706.4:c.-169+747_-169+758del	NM_144706.4:c.-169+748_-169+758del	NM_144706.4:c.-169+749_-169+758del	NM_144706.4:c.-169+750_-169+758del	NM_144706.4:c.-169+752_-169+758del	NM_144706.4:c.-169+753_-169+758del	NM_144706.4:c.-169+754_-169+758del	NM_144706.4:c.-169+755_-169+758del	NM_144706.4:c.-169+756_-169+758del	NM_144706.4:c.-169+757_-169+758del	NM_144706.4:c.-169+758del	NM_144706.4:c.-169+758dup	NM_144706.4:c.-169+757_-169+758dup	NM_144706.4:c.-169+756_-169+758dup	NM_144706.4:c.-169+755_-169+758dup	NM_144706.4:c.-169+754_-169+758dup	NM_144706.4:c.-169+753_-169+758dup
TSGA10 transcript variant X11	XM_017005041.3:c.-529+11559=	XM_017005041.3:c.-529+11545_-529+11559del	XM_017005041.3:c.-529+11546_-529+11559del	XM_017005041.3:c.-529+11547_-529+11559del	XM_017005041.3:c.-529+11548_-529+11559del	XM_017005041.3:c.-529+11549_-529+11559del	XM_017005041.3:c.-529+11550_-529+11559del	XM_017005041.3:c.-529+11551_-529+11559del	XM_017005041.3:c.-529+11553_-529+11559del	XM_017005041.3:c.-529+11554_-529+11559del	XM_017005041.3:c.-529+11555_-529+11559del	XM_017005041.3:c.-529+11556_-529+11559del	XM_017005041.3:c.-529+11557_-529+11559del	XM_017005041.3:c.-529+11558_-529+11559del	XM_017005041.3:c.-529+11559del	XM_017005041.3:c.-529+11559dup	XM_017005041.3:c.-529+11558_-529+11559dup	XM_017005041.3:c.-529+11557_-529+11559dup	XM_017005041.3:c.-529+11556_-529+11559dup	XM_017005041.3:c.-529+11555_-529+11559dup	XM_017005041.3:c.-529+11554_-529+11559dup
TSGA10 transcript variant X3	XM_047445928.1:c.33+11157=	XM_047445928.1:c.33+11143_33+11157del	XM_047445928.1:c.33+11144_33+11157del	XM_047445928.1:c.33+11145_33+11157del	XM_047445928.1:c.33+11146_33+11157del	XM_047445928.1:c.33+11147_33+11157del	XM_047445928.1:c.33+11148_33+11157del	XM_047445928.1:c.33+11149_33+11157del	XM_047445928.1:c.33+11151_33+11157del	XM_047445928.1:c.33+11152_33+11157del	XM_047445928.1:c.33+11153_33+11157del	XM_047445928.1:c.33+11154_33+11157del	XM_047445928.1:c.33+11155_33+11157del	XM_047445928.1:c.33+11156_33+11157del	XM_047445928.1:c.33+11157del	XM_047445928.1:c.33+11157dup	XM_047445928.1:c.33+11156_33+11157dup	XM_047445928.1:c.33+11155_33+11157dup	XM_047445928.1:c.33+11154_33+11157dup	XM_047445928.1:c.33+11153_33+11157dup	XM_047445928.1:c.33+11152_33+11157dup
TSGA10 transcript variant X4	XM_047445929.1:c.33+11157=	XM_047445929.1:c.33+11143_33+11157del	XM_047445929.1:c.33+11144_33+11157del	XM_047445929.1:c.33+11145_33+11157del	XM_047445929.1:c.33+11146_33+11157del	XM_047445929.1:c.33+11147_33+11157del	XM_047445929.1:c.33+11148_33+11157del	XM_047445929.1:c.33+11149_33+11157del	XM_047445929.1:c.33+11151_33+11157del	XM_047445929.1:c.33+11152_33+11157del	XM_047445929.1:c.33+11153_33+11157del	XM_047445929.1:c.33+11154_33+11157del	XM_047445929.1:c.33+11155_33+11157del	XM_047445929.1:c.33+11156_33+11157del	XM_047445929.1:c.33+11157del	XM_047445929.1:c.33+11157dup	XM_047445929.1:c.33+11156_33+11157dup	XM_047445929.1:c.33+11155_33+11157dup	XM_047445929.1:c.33+11154_33+11157dup	XM_047445929.1:c.33+11153_33+11157dup	XM_047445929.1:c.33+11152_33+11157dup
TSGA10 transcript variant X5	XM_047445930.1:c.33+11157=	XM_047445930.1:c.33+11143_33+11157del	XM_047445930.1:c.33+11144_33+11157del	XM_047445930.1:c.33+11145_33+11157del	XM_047445930.1:c.33+11146_33+11157del	XM_047445930.1:c.33+11147_33+11157del	XM_047445930.1:c.33+11148_33+11157del	XM_047445930.1:c.33+11149_33+11157del	XM_047445930.1:c.33+11151_33+11157del	XM_047445930.1:c.33+11152_33+11157del	XM_047445930.1:c.33+11153_33+11157del	XM_047445930.1:c.33+11154_33+11157del	XM_047445930.1:c.33+11155_33+11157del	XM_047445930.1:c.33+11156_33+11157del	XM_047445930.1:c.33+11157del	XM_047445930.1:c.33+11157dup	XM_047445930.1:c.33+11156_33+11157dup	XM_047445930.1:c.33+11155_33+11157dup	XM_047445930.1:c.33+11154_33+11157dup	XM_047445930.1:c.33+11153_33+11157dup	XM_047445930.1:c.33+11152_33+11157dup
TSGA10 transcript variant X6	XM_047445931.1:c.33+11157=	XM_047445931.1:c.33+11143_33+11157del	XM_047445931.1:c.33+11144_33+11157del	XM_047445931.1:c.33+11145_33+11157del	XM_047445931.1:c.33+11146_33+11157del	XM_047445931.1:c.33+11147_33+11157del	XM_047445931.1:c.33+11148_33+11157del	XM_047445931.1:c.33+11149_33+11157del	XM_047445931.1:c.33+11151_33+11157del	XM_047445931.1:c.33+11152_33+11157del	XM_047445931.1:c.33+11153_33+11157del	XM_047445931.1:c.33+11154_33+11157del	XM_047445931.1:c.33+11155_33+11157del	XM_047445931.1:c.33+11156_33+11157del	XM_047445931.1:c.33+11157del	XM_047445931.1:c.33+11157dup	XM_047445931.1:c.33+11156_33+11157dup	XM_047445931.1:c.33+11155_33+11157dup	XM_047445931.1:c.33+11154_33+11157dup	XM_047445931.1:c.33+11153_33+11157dup	XM_047445931.1:c.33+11152_33+11157dup
TSGA10 transcript variant X7	XM_047445932.1:c.33+11157=	XM_047445932.1:c.33+11143_33+11157del	XM_047445932.1:c.33+11144_33+11157del	XM_047445932.1:c.33+11145_33+11157del	XM_047445932.1:c.33+11146_33+11157del	XM_047445932.1:c.33+11147_33+11157del	XM_047445932.1:c.33+11148_33+11157del	XM_047445932.1:c.33+11149_33+11157del	XM_047445932.1:c.33+11151_33+11157del	XM_047445932.1:c.33+11152_33+11157del	XM_047445932.1:c.33+11153_33+11157del	XM_047445932.1:c.33+11154_33+11157del	XM_047445932.1:c.33+11155_33+11157del	XM_047445932.1:c.33+11156_33+11157del	XM_047445932.1:c.33+11157del	XM_047445932.1:c.33+11157dup	XM_047445932.1:c.33+11156_33+11157dup	XM_047445932.1:c.33+11155_33+11157dup	XM_047445932.1:c.33+11154_33+11157dup	XM_047445932.1:c.33+11153_33+11157dup	XM_047445932.1:c.33+11152_33+11157dup
TSGA10 transcript variant X16	XM_047445934.1:c.-400+11703=	XM_047445934.1:c.-400+11689_-400+11703del	XM_047445934.1:c.-400+11690_-400+11703del	XM_047445934.1:c.-400+11691_-400+11703del	XM_047445934.1:c.-400+11692_-400+11703del	XM_047445934.1:c.-400+11693_-400+11703del	XM_047445934.1:c.-400+11694_-400+11703del	XM_047445934.1:c.-400+11695_-400+11703del	XM_047445934.1:c.-400+11697_-400+11703del	XM_047445934.1:c.-400+11698_-400+11703del	XM_047445934.1:c.-400+11699_-400+11703del	XM_047445934.1:c.-400+11700_-400+11703del	XM_047445934.1:c.-400+11701_-400+11703del	XM_047445934.1:c.-400+11702_-400+11703del	XM_047445934.1:c.-400+11703del	XM_047445934.1:c.-400+11703dup	XM_047445934.1:c.-400+11702_-400+11703dup	XM_047445934.1:c.-400+11701_-400+11703dup	XM_047445934.1:c.-400+11700_-400+11703dup	XM_047445934.1:c.-400+11699_-400+11703dup	XM_047445934.1:c.-400+11698_-400+11703dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

60 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41667506	Mar 15, 2016 (147)
2	HGSV	ss77981196	Dec 06, 2007 (129)
3	HUMANGENOME_JCVI	ss95279474	Feb 05, 2009 (130)
4	BCMHGSC_JDW	ss103630247	Mar 15, 2016 (147)
5	PJP	ss294994533	May 09, 2011 (135)
6	EVA_UK10K_TWINSUK	ss1702890691	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1702890697	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710014880	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710014882	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710014912	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710014914	Apr 01, 2015 (144)
12	SWEGEN	ss2990042352	Nov 08, 2017 (151)
13	MCHAISSO	ss3063947242	Nov 08, 2017 (151)
14	MCHAISSO	ss3064799180	Nov 08, 2017 (151)
15	MCHAISSO	ss3064799181	Nov 08, 2017 (151)
16	MCHAISSO	ss3065755214	Nov 08, 2017 (151)
17	EVA_DECODE	ss3704467394	Jul 13, 2019 (153)
18	EVA_DECODE	ss3704467395	Jul 13, 2019 (153)
19	EVA_DECODE	ss3704467396	Jul 13, 2019 (153)
20	EVA_DECODE	ss3704467397	Jul 13, 2019 (153)
21	ACPOP	ss3728676537	Jul 13, 2019 (153)
22	PACBIO	ss3789509093	Jul 13, 2019 (153)
23	PACBIO	ss3794381868	Jul 13, 2019 (153)
24	PACBIO	ss3794381869	Jul 13, 2019 (153)
25	EVA	ss3827114871	Apr 25, 2020 (154)
26	GNOMAD	ss4046888465	Apr 27, 2021 (155)
27	GNOMAD	ss4046888466	Apr 27, 2021 (155)
28	GNOMAD	ss4046888467	Apr 27, 2021 (155)
29	GNOMAD	ss4046888468	Apr 27, 2021 (155)
30	GNOMAD	ss4046888469	Apr 27, 2021 (155)
31	GNOMAD	ss4046888470	Apr 27, 2021 (155)
32	GNOMAD	ss4046888472	Apr 27, 2021 (155)
33	GNOMAD	ss4046888473	Apr 27, 2021 (155)
34	GNOMAD	ss4046888474	Apr 27, 2021 (155)
35	GNOMAD	ss4046888475	Apr 27, 2021 (155)
36	GNOMAD	ss4046888476	Apr 27, 2021 (155)
37	GNOMAD	ss4046888477	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5152817842	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5152817843	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5152817844	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5152817845	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5152817846	Apr 27, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5249211468	Oct 12, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5249211469	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5249211470	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5249211471	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5449156248	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5449156249	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5449156250	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5449156251	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5449156252	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5449156253	Oct 12, 2022 (156)
53	SANFORD_IMAGENETICS	ss5629345443	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5682636632	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5682636633	Oct 12, 2022 (156)
56	TOMMO_GENOMICS	ss5682636634	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5682636635	Oct 12, 2022 (156)
58	TOMMO_GENOMICS	ss5682636636	Oct 12, 2022 (156)
59	EVA	ss5820495799	Oct 12, 2022 (156)
60	EVA	ss5820495800	Oct 12, 2022 (156)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 5197304 (NC_000002.11:99759598:T: 2150/3854) Row 5197305 (NC_000002.11:99759597:TTT: 1170/3854) Row 5197306 (NC_000002.11:99759596:TTTTT: 362/3854)	-	Oct 11, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 5197304 (NC_000002.11:99759598:T: 2150/3854) Row 5197305 (NC_000002.11:99759597:TTT: 1170/3854) Row 5197306 (NC_000002.11:99759596:TTTTT: 362/3854)	-	Oct 11, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 5197304 (NC_000002.11:99759598:T: 2150/3854) Row 5197305 (NC_000002.11:99759597:TTT: 1170/3854) Row 5197306 (NC_000002.11:99759596:TTTTT: 362/3854)	-	Oct 11, 2018 (152)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 67255001 (NC_000002.12:99143133::T 898/77698) Row 67255002 (NC_000002.12:99143133::TT 42/77718) Row 67255003 (NC_000002.12:99143133::TTT 17/77720)...	-	Apr 27, 2021 (155)
77	Northern Sweden	NC_000002.11 - 99759597	Jul 13, 2019 (153)
78	8.3KJPN Submission ignored due to conflicting rows: Row 10787149 (NC_000002.11:99759596:TTT: 5073/16446) Row 10787150 (NC_000002.11:99759596:TT: 1770/16446) Row 10787151 (NC_000002.11:99759596:TTTTTTTTTT: 6/16446)...	-	Apr 27, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 10787149 (NC_000002.11:99759596:TTT: 5073/16446) Row 10787150 (NC_000002.11:99759596:TT: 1770/16446) Row 10787151 (NC_000002.11:99759596:TTTTTTTTTT: 6/16446)...	-	Apr 27, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 10787149 (NC_000002.11:99759596:TTT: 5073/16446) Row 10787150 (NC_000002.11:99759596:TT: 1770/16446) Row 10787151 (NC_000002.11:99759596:TTTTTTTTTT: 6/16446)...	-	Apr 27, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 10787149 (NC_000002.11:99759596:TTT: 5073/16446) Row 10787150 (NC_000002.11:99759596:TT: 1770/16446) Row 10787151 (NC_000002.11:99759596:TTTTTTTTTT: 6/16446)...	-	Apr 27, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 10787149 (NC_000002.11:99759596:TTT: 5073/16446) Row 10787150 (NC_000002.11:99759596:TT: 1770/16446) Row 10787151 (NC_000002.11:99759596:TTTTTTTTTT: 6/16446)...	-	Apr 27, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 16473736 (NC_000002.12:99143133:TTT: 11900/27298) Row 16473737 (NC_000002.12:99143133:TT: 4299/27298) Row 16473738 (NC_000002.12:99143133:TTTTTTTTTT: 9/27298)...	-	Oct 12, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 16473736 (NC_000002.12:99143133:TTT: 11900/27298) Row 16473737 (NC_000002.12:99143133:TT: 4299/27298) Row 16473738 (NC_000002.12:99143133:TTTTTTTTTT: 9/27298)...	-	Oct 12, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 16473736 (NC_000002.12:99143133:TTT: 11900/27298) Row 16473737 (NC_000002.12:99143133:TT: 4299/27298) Row 16473738 (NC_000002.12:99143133:TTTTTTTTTT: 9/27298)...	-	Oct 12, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 16473736 (NC_000002.12:99143133:TTT: 11900/27298) Row 16473737 (NC_000002.12:99143133:TT: 4299/27298) Row 16473738 (NC_000002.12:99143133:TTTTTTTTTT: 9/27298)...	-	Oct 12, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 16473736 (NC_000002.12:99143133:TTT: 11900/27298) Row 16473737 (NC_000002.12:99143133:TT: 4299/27298) Row 16473738 (NC_000002.12:99143133:TTTTTTTTTT: 9/27298)...	-	Oct 12, 2022 (156)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 5197304 (NC_000002.11:99759598:T: 2106/3708) Row 5197305 (NC_000002.11:99759597:TTT: 1091/3708) Row 5197306 (NC_000002.11:99759596:TTTTT: 359/3708)	-	Oct 11, 2018 (152)
89	UK 10K study - Twins Submission ignored due to conflicting rows: Row 5197304 (NC_000002.11:99759598:T: 2106/3708) Row 5197305 (NC_000002.11:99759597:TTT: 1091/3708) Row 5197306 (NC_000002.11:99759596:TTTTT: 359/3708)	-	Oct 11, 2018 (152)
90	UK 10K study - Twins Submission ignored due to conflicting rows: Row 5197304 (NC_000002.11:99759598:T: 2106/3708) Row 5197305 (NC_000002.11:99759597:TTT: 1091/3708) Row 5197306 (NC_000002.11:99759596:TTTTT: 359/3708)	-	Oct 11, 2018 (152)
91	ALFA	NC_000002.12 - 99143134	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs36172340	Apr 25, 2013 (138)
rs72349807	Oct 13, 2011 (136)
rs146032347	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4046888477	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5629345443	NC_000002.11:99759596:TTTTTTTTTTTT… NC_000002.11:99759596:TTTTTTTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT
ss4046888476, ss5249211470, ss5449156252	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4046888475	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4046888474	NC_000002.12:99143133:TTTTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5152817844	NC_000002.11:99759596:TTTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4046888473, ss5682636634	NC_000002.12:99143133:TTTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4046888472	NC_000002.12:99143133:TTTTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1702890691, ss1702890697	NC_000002.11:99759596:TTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5152817845, ss5820495800	NC_000002.11:99759596:TTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710014882, ss1710014914	NC_000002.11:99759597:TTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3704467394, ss5249211469, ss5449156250, ss5682636635	NC_000002.12:99143133:TTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss41667506	NT_022171.15:4433425:TTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss77981196	NC_000002.9:99218137:TTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294994533	NC_000002.10:99126051:TTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1961402, ss2990042352, ss3728676537, ss3789509093, ss3794381868, ss5152817842, ss5820495799	NC_000002.11:99759596:TTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000002.11:99759597:TTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710014880, ss1710014912	NC_000002.11:99759598:TTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3063947242, ss3064799180, ss3065755214, ss5449156248, ss5682636632	NC_000002.12:99143133:TTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3704467395	NC_000002.12:99143134:TTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss41667506	NT_022171.15:4433425:TTTT:T	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3794381869, ss3827114871, ss5152817843	NC_000002.11:99759596:TT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3064799181, ss5449156249, ss5682636633	NC_000002.12:99143133:TT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3704467396	NC_000002.12:99143135:TT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5152817846	NC_000002.11:99759596:T:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000002.11:99759598:T:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5249211468, ss5449156251, ss5682636636	NC_000002.12:99143133:T:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103630247	NT_022171.15:4433449:T:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95279474	NT_022171.15:4433450:T:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4046888465, ss5249211471, ss5449156253	NC_000002.12:99143133::T	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3704467397	NC_000002.12:99143137::T	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4046888466	NC_000002.12:99143133::TT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95279474	NT_022171.15:4433450:T:TTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4046888467	NC_000002.12:99143133::TTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103630247	NT_022171.15:4433449:T:TTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4046888468	NC_000002.12:99143133::TTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1393054225	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4046888469	NC_000002.12:99143133::TTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4046888470	NC_000002.12:99143133::TTTTTT	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3317026703	NC_000002.12:99143133:TTTTTTT:	NC_000002.12:99143133:TTTTTTTTTTTT… NC_000002.12:99143133:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs10605521

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10605521