Name: rs71208595
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.

rs71208595

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:23224300-23224322 (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(A)₁₆ / del(A)₁₅ / del(A)₁₄ / d…
del(A)₁₆ / del(A)₁₅ / del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₉ / dup(A)₁₄ / dup(A)₁₇ / dup(A)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: (A)₂₃=0.0381 (191/5008, 1000G)
del(A)₁₆=0.000 (0/114, ALFA)
del(A)₁₅=0.000 (0/114, ALFA) (+ 19 more)
del(A)₁₄=0.000 (0/114, ALFA)
del(A)₁₃=0.000 (0/114, ALFA)
del(A)₁₂=0.000 (0/114, ALFA)
del(A)₁₁=0.000 (0/114, ALFA)
del(A)₁₀=0.000 (0/114, ALFA)
del(A)₉=0.000 (0/114, ALFA)
del(A)₈=0.000 (0/114, ALFA)
del(A)₇=0.000 (0/114, ALFA)
del(A)₆=0.000 (0/114, ALFA)
del(A)₅=0.000 (0/114, ALFA)
del(A)₄=0.000 (0/114, ALFA)
delAAA=0.000 (0/114, ALFA)
delAA=0.000 (0/114, ALFA)
delA=0.000 (0/114, ALFA)
dupA=0.000 (0/114, ALFA)
dupAA=0.000 (0/114, ALFA)
dupAAA=0.000 (0/114, ALFA)
dup(A)₄=0.000 (0/114, ALFA)
(A)₂₃=0.00 (0/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TNFRSF10A : Intron Variant
TNFRSF10A-DT : 2KB Upstream 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	114	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	60	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	48	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	48	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	6	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAA=0.0, AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₃=0.0381	del(A)₁₀=0.9619
1000Genomes	African	Sub	1322	(A)₂₃=0.0719	del(A)₁₀=0.9281
1000Genomes	East Asian	Sub	1008	(A)₂₃=0.0327	del(A)₁₀=0.9673
1000Genomes	Europe	Sub	1006	(A)₂₃=0.0338	del(A)₁₀=0.9662
1000Genomes	South Asian	Sub	978	(A)₂₃=0.008	del(A)₁₀=0.992
1000Genomes	American	Sub	694	(A)₂₃=0.030	del(A)₁₀=0.970
Allele Frequency Aggregator	Total	Global	114	(A)₂₃=1.000	del(A)₁₆=0.000, del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	European	Sub	60	(A)₂₃=1.00	del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	African	Sub	48	(A)₂₃=1.00	del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Other	Sub	6	(A)₂₃=1.0	del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₂₃=0	del(A)₁₆=0, del(A)₁₅=0, del(A)₁₄=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₂₃=0	del(A)₁₆=0, del(A)₁₅=0, del(A)₁₄=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₃=0	del(A)₁₆=0, del(A)₁₅=0, del(A)₁₄=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₂₃=0	del(A)₁₆=0, del(A)₁₅=0, del(A)₁₄=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0
The Danish reference pan genome	Danish	Study-wide	40	(A)₂₃=0.00	del(A)₉=1.00

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 8	NC_000008.11:g.23224307_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224308_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224309_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224310_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224311_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224312_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224313_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224314_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224315_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224316_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224317_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224318_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224319_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224320_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224321_23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224322del
GRCh38.p14 chr 8	NC_000008.11:g.23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224321_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224320_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224319_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224318_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224317_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224316_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224314_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224309_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224306_23224322dup
GRCh38.p14 chr 8	NC_000008.11:g.23224305_23224322dup
GRCh37.p13 chr 8	NC_000008.10:g.23081820_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081821_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081822_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081823_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081824_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081825_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081826_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081827_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081828_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081829_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081830_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081831_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081832_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081833_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081834_23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081835del
GRCh37.p13 chr 8	NC_000008.10:g.23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081834_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081833_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081832_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081831_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081830_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081829_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081827_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081822_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081819_23081835dup
GRCh37.p13 chr 8	NC_000008.10:g.23081818_23081835dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5853_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5854_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5855_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5856_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5857_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5858_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5859_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5860_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5861_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5862_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5863_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5864_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5865_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5866_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5867_5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5868del
TNFRSF10A RefSeqGene	NG_032107.1:g.5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5867_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5866_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5865_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5864_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5863_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5862_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5860_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5855_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5852_5868dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5851_5868dup

Gene: TNFRSF10A, TNF receptor superfamily member 10a (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TNFRSF10A transcript	NM_003844.4:c.306+441_306… NM_003844.4:c.306+441_306+456del	N/A	Intron Variant

Gene: TNFRSF10A-DT, TNFRSF10A divergent transcript (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TNFRSF10A-DT transcript	NR_033928.1:n.	N/A	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	(A)₂₃=	del(A)₁₆	del(A)₁₅	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₉	dup(A)₁₄	dup(A)₁₇	dup(A)₁₈
GRCh38.p14 chr 8	NC_000008.11:g.23224300_23224322=	NC_000008.11:g.23224307_23224322del	NC_000008.11:g.23224308_23224322del	NC_000008.11:g.23224309_23224322del	NC_000008.11:g.23224310_23224322del	NC_000008.11:g.23224311_23224322del	NC_000008.11:g.23224312_23224322del	NC_000008.11:g.23224313_23224322del	NC_000008.11:g.23224314_23224322del	NC_000008.11:g.23224315_23224322del	NC_000008.11:g.23224316_23224322del	NC_000008.11:g.23224317_23224322del	NC_000008.11:g.23224318_23224322del	NC_000008.11:g.23224319_23224322del	NC_000008.11:g.23224320_23224322del	NC_000008.11:g.23224321_23224322del	NC_000008.11:g.23224322del	NC_000008.11:g.23224322dup	NC_000008.11:g.23224321_23224322dup	NC_000008.11:g.23224320_23224322dup	NC_000008.11:g.23224319_23224322dup	NC_000008.11:g.23224318_23224322dup	NC_000008.11:g.23224317_23224322dup	NC_000008.11:g.23224316_23224322dup	NC_000008.11:g.23224314_23224322dup	NC_000008.11:g.23224309_23224322dup	NC_000008.11:g.23224306_23224322dup	NC_000008.11:g.23224305_23224322dup
GRCh37.p13 chr 8	NC_000008.10:g.23081813_23081835=	NC_000008.10:g.23081820_23081835del	NC_000008.10:g.23081821_23081835del	NC_000008.10:g.23081822_23081835del	NC_000008.10:g.23081823_23081835del	NC_000008.10:g.23081824_23081835del	NC_000008.10:g.23081825_23081835del	NC_000008.10:g.23081826_23081835del	NC_000008.10:g.23081827_23081835del	NC_000008.10:g.23081828_23081835del	NC_000008.10:g.23081829_23081835del	NC_000008.10:g.23081830_23081835del	NC_000008.10:g.23081831_23081835del	NC_000008.10:g.23081832_23081835del	NC_000008.10:g.23081833_23081835del	NC_000008.10:g.23081834_23081835del	NC_000008.10:g.23081835del	NC_000008.10:g.23081835dup	NC_000008.10:g.23081834_23081835dup	NC_000008.10:g.23081833_23081835dup	NC_000008.10:g.23081832_23081835dup	NC_000008.10:g.23081831_23081835dup	NC_000008.10:g.23081830_23081835dup	NC_000008.10:g.23081829_23081835dup	NC_000008.10:g.23081827_23081835dup	NC_000008.10:g.23081822_23081835dup	NC_000008.10:g.23081819_23081835dup	NC_000008.10:g.23081818_23081835dup
TNFRSF10A RefSeqGene	NG_032107.1:g.5846_5868=	NG_032107.1:g.5853_5868del	NG_032107.1:g.5854_5868del	NG_032107.1:g.5855_5868del	NG_032107.1:g.5856_5868del	NG_032107.1:g.5857_5868del	NG_032107.1:g.5858_5868del	NG_032107.1:g.5859_5868del	NG_032107.1:g.5860_5868del	NG_032107.1:g.5861_5868del	NG_032107.1:g.5862_5868del	NG_032107.1:g.5863_5868del	NG_032107.1:g.5864_5868del	NG_032107.1:g.5865_5868del	NG_032107.1:g.5866_5868del	NG_032107.1:g.5867_5868del	NG_032107.1:g.5868del	NG_032107.1:g.5868dup	NG_032107.1:g.5867_5868dup	NG_032107.1:g.5866_5868dup	NG_032107.1:g.5865_5868dup	NG_032107.1:g.5864_5868dup	NG_032107.1:g.5863_5868dup	NG_032107.1:g.5862_5868dup	NG_032107.1:g.5860_5868dup	NG_032107.1:g.5855_5868dup	NG_032107.1:g.5852_5868dup	NG_032107.1:g.5851_5868dup
TNFRSF10A transcript	NM_003844.3:c.306+456=	NM_003844.3:c.306+441_306+456del	NM_003844.3:c.306+442_306+456del	NM_003844.3:c.306+443_306+456del	NM_003844.3:c.306+444_306+456del	NM_003844.3:c.306+445_306+456del	NM_003844.3:c.306+446_306+456del	NM_003844.3:c.306+447_306+456del	NM_003844.3:c.306+448_306+456del	NM_003844.3:c.306+449_306+456del	NM_003844.3:c.306+450_306+456del	NM_003844.3:c.306+451_306+456del	NM_003844.3:c.306+452_306+456del	NM_003844.3:c.306+453_306+456del	NM_003844.3:c.306+454_306+456del	NM_003844.3:c.306+455_306+456del	NM_003844.3:c.306+456del	NM_003844.3:c.306+456dup	NM_003844.3:c.306+455_306+456dup	NM_003844.3:c.306+454_306+456dup	NM_003844.3:c.306+453_306+456dup	NM_003844.3:c.306+452_306+456dup	NM_003844.3:c.306+451_306+456dup	NM_003844.3:c.306+450_306+456dup	NM_003844.3:c.306+448_306+456dup	NM_003844.3:c.306+443_306+456dup	NM_003844.3:c.306+440_306+456dup	NM_003844.3:c.306+439_306+456dup
TNFRSF10A transcript	NM_003844.4:c.306+456=	NM_003844.4:c.306+441_306+456del	NM_003844.4:c.306+442_306+456del	NM_003844.4:c.306+443_306+456del	NM_003844.4:c.306+444_306+456del	NM_003844.4:c.306+445_306+456del	NM_003844.4:c.306+446_306+456del	NM_003844.4:c.306+447_306+456del	NM_003844.4:c.306+448_306+456del	NM_003844.4:c.306+449_306+456del	NM_003844.4:c.306+450_306+456del	NM_003844.4:c.306+451_306+456del	NM_003844.4:c.306+452_306+456del	NM_003844.4:c.306+453_306+456del	NM_003844.4:c.306+454_306+456del	NM_003844.4:c.306+455_306+456del	NM_003844.4:c.306+456del	NM_003844.4:c.306+456dup	NM_003844.4:c.306+455_306+456dup	NM_003844.4:c.306+454_306+456dup	NM_003844.4:c.306+453_306+456dup	NM_003844.4:c.306+452_306+456dup	NM_003844.4:c.306+451_306+456dup	NM_003844.4:c.306+450_306+456dup	NM_003844.4:c.306+448_306+456dup	NM_003844.4:c.306+443_306+456dup	NM_003844.4:c.306+440_306+456dup	NM_003844.4:c.306+439_306+456dup

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#.

72 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95486908	Feb 13, 2009 (130)
2	BUSHMAN	ss193966992	Apr 25, 2013 (138)
3	1000GENOMES	ss1367869397	Aug 21, 2014 (142)
4	EVA_GENOME_DK	ss1583578249	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1705979755	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1705979771	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1710371757	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710371758	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710371773	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710371775	Apr 01, 2015 (144)
11	SYSTEMSBIOZJU	ss2626981914	Nov 08, 2017 (151)
12	SWEGEN	ss3002846636	Nov 08, 2017 (151)
13	MCHAISSO	ss3064292895	Nov 08, 2017 (151)
14	MCHAISSO	ss3066192622	Nov 08, 2017 (151)
15	EVA_DECODE	ss3721611171	Jul 13, 2019 (153)
16	EVA_DECODE	ss3721611172	Jul 13, 2019 (153)
17	EVA_DECODE	ss3721611173	Jul 13, 2019 (153)
18	EVA_DECODE	ss3721611174	Jul 13, 2019 (153)
19	EVA_DECODE	ss3721611175	Jul 13, 2019 (153)
20	EVA_DECODE	ss3721611176	Jul 13, 2019 (153)
21	INMEGENXS	ss3745700840	Jul 13, 2019 (153)
22	PACBIO	ss3791359153	Jul 13, 2019 (153)
23	PACBIO	ss3796240338	Jul 13, 2019 (153)
24	PACBIO	ss3796240339	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3810914702	Jul 13, 2019 (153)
26	GNOMAD	ss4180790683	Apr 26, 2021 (155)
27	GNOMAD	ss4180790684	Apr 26, 2021 (155)
28	GNOMAD	ss4180790685	Apr 26, 2021 (155)
29	GNOMAD	ss4180790686	Apr 26, 2021 (155)
30	GNOMAD	ss4180790687	Apr 26, 2021 (155)
31	GNOMAD	ss4180790688	Apr 26, 2021 (155)
32	GNOMAD	ss4180790689	Apr 26, 2021 (155)
33	GNOMAD	ss4180790690	Apr 26, 2021 (155)
34	GNOMAD	ss4180790691	Apr 26, 2021 (155)
35	GNOMAD	ss4180790693	Apr 26, 2021 (155)
36	GNOMAD	ss4180790694	Apr 26, 2021 (155)
37	GNOMAD	ss4180790695	Apr 26, 2021 (155)
38	GNOMAD	ss4180790696	Apr 26, 2021 (155)
39	GNOMAD	ss4180790697	Apr 26, 2021 (155)
40	GNOMAD	ss4180790698	Apr 26, 2021 (155)
41	GNOMAD	ss4180790699	Apr 26, 2021 (155)
42	GNOMAD	ss4180790700	Apr 26, 2021 (155)
43	GNOMAD	ss4180790701	Apr 26, 2021 (155)
44	GNOMAD	ss4180790702	Apr 26, 2021 (155)
45	GNOMAD	ss4180790703	Apr 26, 2021 (155)
46	GNOMAD	ss4180790704	Apr 26, 2021 (155)
47	GNOMAD	ss4180790705	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5187774055	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5187774056	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5187774057	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5187774058	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5187774059	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5187774060	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5276427173	Oct 14, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5276427174	Oct 14, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5276427175	Oct 14, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5276427176	Oct 14, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5276427177	Oct 14, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5276427178	Oct 14, 2022 (156)
60	HUGCELL_USP	ss5473067989	Oct 14, 2022 (156)
61	HUGCELL_USP	ss5473067990	Oct 14, 2022 (156)
62	HUGCELL_USP	ss5473067991	Oct 14, 2022 (156)
63	TOMMO_GENOMICS	ss5729427150	Oct 14, 2022 (156)
64	TOMMO_GENOMICS	ss5729427151	Oct 14, 2022 (156)
65	TOMMO_GENOMICS	ss5729427152	Oct 14, 2022 (156)
66	TOMMO_GENOMICS	ss5729427153	Oct 14, 2022 (156)
67	TOMMO_GENOMICS	ss5729427154	Oct 14, 2022 (156)
68	TOMMO_GENOMICS	ss5729427155	Oct 14, 2022 (156)
69	EVA	ss5830260766	Oct 14, 2022 (156)
70	EVA	ss5830260767	Oct 14, 2022 (156)
71	EVA	ss5856298345	Oct 14, 2022 (156)
72	EVA	ss5888135140	Oct 14, 2022 (156)
73	1000Genomes	NC_000008.10 - 23081813	Oct 12, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 22862473 (NC_000008.10:23081812:AAAAAAAAAA: 2678/3854) Row 22862475 (NC_000008.10:23081813:AAAAAAAA: 214/3854)	-	Oct 12, 2018 (152)
75	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 22862473 (NC_000008.10:23081812:AAAAAAAAAA: 2678/3854) Row 22862475 (NC_000008.10:23081813:AAAAAAAA: 214/3854)	-	Oct 12, 2018 (152)
76	The Danish reference pan genome	NC_000008.10 - 23081814	Apr 26, 2020 (154)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289975729 (NC_000008.11:23224299::AAA 88/91644) Row 289975730 (NC_000008.11:23224299::AAAA 19/91642) Row 289975731 (NC_000008.11:23224299::AAAAA 6/91654)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 45743362 (NC_000008.10:23081812:AAAAAAAAAA: 11931/16482) Row 45743363 (NC_000008.10:23081812:AA: 2239/16482) Row 45743364 (NC_000008.10:23081812:AAAAAAAAAAAAAA: 645/16482)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 45743362 (NC_000008.10:23081812:AAAAAAAAAA: 11931/16482) Row 45743363 (NC_000008.10:23081812:AA: 2239/16482) Row 45743364 (NC_000008.10:23081812:AAAAAAAAAAAAAA: 645/16482)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 45743362 (NC_000008.10:23081812:AAAAAAAAAA: 11931/16482) Row 45743363 (NC_000008.10:23081812:AA: 2239/16482) Row 45743364 (NC_000008.10:23081812:AAAAAAAAAAAAAA: 645/16482)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 45743362 (NC_000008.10:23081812:AAAAAAAAAA: 11931/16482) Row 45743363 (NC_000008.10:23081812:AA: 2239/16482) Row 45743364 (NC_000008.10:23081812:AAAAAAAAAAAAAA: 645/16482)...	-	Apr 26, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 45743362 (NC_000008.10:23081812:AAAAAAAAAA: 11931/16482) Row 45743363 (NC_000008.10:23081812:AA: 2239/16482) Row 45743364 (NC_000008.10:23081812:AAAAAAAAAAAAAA: 645/16482)...	-	Apr 26, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 45743362 (NC_000008.10:23081812:AAAAAAAAAA: 11931/16482) Row 45743363 (NC_000008.10:23081812:AA: 2239/16482) Row 45743364 (NC_000008.10:23081812:AAAAAAAAAAAAAA: 645/16482)...	-	Apr 26, 2021 (155)
105	14KJPN Submission ignored due to conflicting rows: Row 63264254 (NC_000008.11:23224299:AAAAAAAAAA: 20139/26850) Row 63264255 (NC_000008.11:23224299:AA: 3302/26850) Row 63264256 (NC_000008.11:23224299:AAAAAAAAAAAAAA: 1186/26850)...	-	Oct 14, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 63264254 (NC_000008.11:23224299:AAAAAAAAAA: 20139/26850) Row 63264255 (NC_000008.11:23224299:AA: 3302/26850) Row 63264256 (NC_000008.11:23224299:AAAAAAAAAAAAAA: 1186/26850)...	-	Oct 14, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 63264254 (NC_000008.11:23224299:AAAAAAAAAA: 20139/26850) Row 63264255 (NC_000008.11:23224299:AA: 3302/26850) Row 63264256 (NC_000008.11:23224299:AAAAAAAAAAAAAA: 1186/26850)...	-	Oct 14, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 63264254 (NC_000008.11:23224299:AAAAAAAAAA: 20139/26850) Row 63264255 (NC_000008.11:23224299:AA: 3302/26850) Row 63264256 (NC_000008.11:23224299:AAAAAAAAAAAAAA: 1186/26850)...	-	Oct 14, 2022 (156)
109	14KJPN Submission ignored due to conflicting rows: Row 63264254 (NC_000008.11:23224299:AAAAAAAAAA: 20139/26850) Row 63264255 (NC_000008.11:23224299:AA: 3302/26850) Row 63264256 (NC_000008.11:23224299:AAAAAAAAAAAAAA: 1186/26850)...	-	Oct 14, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 63264254 (NC_000008.11:23224299:AAAAAAAAAA: 20139/26850) Row 63264255 (NC_000008.11:23224299:AA: 3302/26850) Row 63264256 (NC_000008.11:23224299:AAAAAAAAAAAAAA: 1186/26850)...	-	Oct 14, 2022 (156)
111	UK 10K study - Twins Submission ignored due to conflicting rows: Row 22862473 (NC_000008.10:23081812:AAAAAAAAAA: 2605/3708) Row 22862475 (NC_000008.10:23081813:AAAAAAAA: 169/3708)	-	Oct 12, 2018 (152)
112	UK 10K study - Twins Submission ignored due to conflicting rows: Row 22862473 (NC_000008.10:23081812:AAAAAAAAAA: 2605/3708) Row 22862474 (NC_000008.10:23081820:AA: 886/3708) Row 22862475 (NC_000008.10:23081813:AAAAAAAAA: 169/3708)	-	Apr 26, 2020 (154)
113	UK 10K study - Twins Submission ignored due to conflicting rows: Row 22862473 (NC_000008.10:23081812:AAAAAAAAAA: 2605/3708) Row 22862475 (NC_000008.10:23081813:AAAAAAAA: 169/3708)	-	Oct 12, 2018 (152)
114	ALFA	NC_000008.11 - 23224300	Apr 26, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4180790705	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss3002846636, ss5187774057	NC_000008.10:23081812:AAAAAAAAAAAA… NC_000008.10:23081812:AAAAAAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4180790704, ss5276427178, ss5729427152	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4180790703	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4180790702	NC_000008.11:23224299:AAAAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss5187774058	NC_000008.10:23081812:AAAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3721611176, ss4180790701, ss5729427155	NC_000008.11:23224299:AAAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
41124010, ss1367869397, ss1705979755, ss1705979771, ss2626981914, ss3745700840, ss5187774055, ss5830260766	NC_000008.10:23081812:AAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1583578249	NC_000008.10:23081814:AAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3064292895, ss3066192622, ss3810914702, ss4180790700, ss5276427173, ss5473067989, ss5729427150, ss5856298345, ss5888135140	NC_000008.11:23224299:AAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3721611175	NC_000008.11:23224300:AAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss193966992	NT_167187.2:10939954:AAAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5187774060, ss5830260767	NC_000008.10:23081812:AAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
105819, ss1710371758, ss1710371775	NC_000008.10:23081813:AAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4180790699, ss5729427153	NC_000008.11:23224299:AAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3721611174	NC_000008.11:23224301:AAAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
	NC_000008.10:23081813:AAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4180790698	NC_000008.11:23224299:AAAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4180790697	NC_000008.11:23224299:AAAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4180790696	NC_000008.11:23224299:AAAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4180790695	NC_000008.11:23224299:AAAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4180790694	NC_000008.11:23224299:AAAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4180790693	NC_000008.11:23224299:AAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3721611173	NC_000008.11:23224307:AAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss95486908	NT_167187.1:10939978:AAA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3796240338, ss5187774056	NC_000008.10:23081812:AA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss1710371757, ss1710371773	NC_000008.10:23081820:AA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5276427174, ss5473067991, ss5729427151	NC_000008.11:23224299:AA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3721611172	NC_000008.11:23224308:AA:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3791359153, ss3796240339, ss5187774059	NC_000008.10:23081812:A:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5276427175, ss5473067990, ss5729427154	NC_000008.11:23224299:A:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3721611171	NC_000008.11:23224309:A:	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5276427176	NC_000008.11:23224299::A	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5276427177	NC_000008.11:23224299::AA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790683	NC_000008.11:23224299::AAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790684	NC_000008.11:23224299::AAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10003264237	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790685	NC_000008.11:23224299::AAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790686	NC_000008.11:23224299::AAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790687	NC_000008.11:23224299::AAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790688	NC_000008.11:23224299::AAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790689	NC_000008.11:23224299::AAAAAAAAAAA… NC_000008.11:23224299::AAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790690	NC_000008.11:23224299::AAAAAAAAAAA… NC_000008.11:23224299::AAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180790691	NC_000008.11:23224299::AAAAAAAAAAA… NC_000008.11:23224299::AAAAAAAAAAAAAAAAAA	NC_000008.11:23224299:AAAAAAAAAAAA… NC_000008.11:23224299:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

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

No publications for rs71208595

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

rs71208595