Name: rs70993246
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.

rs70993246

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:21510293-21510308 (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)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / ins(T)₁₇ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₆ / ins(T)₂₉
Variation Type: Indel Insertion and Deletion
Frequency: dup(T)₇=0.08900 (924/10382, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00581 : 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	10382	TTTTTTTTTTTTTTTT=0.89992	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00164, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.08900, TTTTTTTTTTTTTTTTTTTTTTTT=0.00482, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00193, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00116, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00154, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.85001	0.026538	0.123452	32
European	Sub	8558	TTTTTTTTTTTTTTTT=0.8789	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.1076, TTTTTTTTTTTTTTTTTTTTTTTT=0.0058, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0023, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.817964	0.032335	0.149701	32
African	Sub	1284	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	60	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1224	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	80	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	176	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	42	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	238	TTTTTTTTTTTTTTTT=0.987	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.013, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.97479	0.0	0.02521	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	10382	(T)₁₆=0.89992	del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00164, dupTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.08900, dup(T)₈=0.00482, dup(T)₉=0.00000, dup(T)₁₁=0.00154, dup(T)₁₂=0.00116, dup(T)₁₆=0.00193
Allele Frequency Aggregator	European	Sub	8558	(T)₁₆=0.8789	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0020, dupTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.1076, dup(T)₈=0.0058, dup(T)₉=0.0000, dup(T)₁₁=0.0019, dup(T)₁₂=0.0014, dup(T)₁₆=0.0023
Allele Frequency Aggregator	African	Sub	1284	(T)₁₆=1.0000	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₁=0.0000, dup(T)₁₂=0.0000, dup(T)₁₆=0.0000
Allele Frequency Aggregator	Other	Sub	238	(T)₁₆=0.987	del(T)₅=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, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.013, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	176	(T)₁₆=1.000	del(T)₅=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, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	80	(T)₁₆=1.00	del(T)₅=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, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₆=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(T)₁₆=1.00	del(T)₅=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, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₆=0.00
Allele Frequency Aggregator	Asian	Sub	4	(T)₁₆=1.0	del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0, dup(T)₉=0.0, dup(T)₁₁=0.0, dup(T)₁₂=0.0, dup(T)₁₆=0.0

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 6	NC_000006.12:g.21510304_21510308del
GRCh38.p14 chr 6	NC_000006.12:g.21510305_21510308del
GRCh38.p14 chr 6	NC_000006.12:g.21510306_21510308del
GRCh38.p14 chr 6	NC_000006.12:g.21510307_21510308del
GRCh38.p14 chr 6	NC_000006.12:g.21510308del
GRCh38.p14 chr 6	NC_000006.12:g.21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510307_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510306_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510305_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510304_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510303_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510302_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510301_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510300_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510299_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510298_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510297_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510296_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510295_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510294_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510293_21510308dup
GRCh38.p14 chr 6	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510535_21510539del
GRCh37.p13 chr 6	NC_000006.11:g.21510536_21510539del
GRCh37.p13 chr 6	NC_000006.11:g.21510537_21510539del
GRCh37.p13 chr 6	NC_000006.11:g.21510538_21510539del
GRCh37.p13 chr 6	NC_000006.11:g.21510539del
GRCh37.p13 chr 6	NC_000006.11:g.21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510538_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510537_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510536_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510535_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510534_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510533_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510532_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510531_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510530_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510529_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510528_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510527_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510526_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510525_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510524_21510539dup
GRCh37.p13 chr 6	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LINC00581, long intergenic non-protein coding RNA 581 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00581 transcript	NR_103790.1:n.	N/A	Intron 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)₁₆=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	ins(T)₁₇	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀	ins(T)₂₁	ins(T)₂₆	ins(T)₂₉
GRCh38.p14 chr 6	NC_000006.12:g.21510293_21510308=	NC_000006.12:g.21510304_21510308del	NC_000006.12:g.21510305_21510308del	NC_000006.12:g.21510306_21510308del	NC_000006.12:g.21510307_21510308del	NC_000006.12:g.21510308del	NC_000006.12:g.21510308dup	NC_000006.12:g.21510307_21510308dup	NC_000006.12:g.21510306_21510308dup	NC_000006.12:g.21510305_21510308dup	NC_000006.12:g.21510304_21510308dup	NC_000006.12:g.21510303_21510308dup	NC_000006.12:g.21510302_21510308dup	NC_000006.12:g.21510301_21510308dup	NC_000006.12:g.21510300_21510308dup	NC_000006.12:g.21510299_21510308dup	NC_000006.12:g.21510298_21510308dup	NC_000006.12:g.21510297_21510308dup	NC_000006.12:g.21510296_21510308dup	NC_000006.12:g.21510295_21510308dup	NC_000006.12:g.21510294_21510308dup	NC_000006.12:g.21510293_21510308dup	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTT	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTT	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.21510308_21510309insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.21510524_21510539=	NC_000006.11:g.21510535_21510539del	NC_000006.11:g.21510536_21510539del	NC_000006.11:g.21510537_21510539del	NC_000006.11:g.21510538_21510539del	NC_000006.11:g.21510539del	NC_000006.11:g.21510539dup	NC_000006.11:g.21510538_21510539dup	NC_000006.11:g.21510537_21510539dup	NC_000006.11:g.21510536_21510539dup	NC_000006.11:g.21510535_21510539dup	NC_000006.11:g.21510534_21510539dup	NC_000006.11:g.21510533_21510539dup	NC_000006.11:g.21510532_21510539dup	NC_000006.11:g.21510531_21510539dup	NC_000006.11:g.21510530_21510539dup	NC_000006.11:g.21510529_21510539dup	NC_000006.11:g.21510528_21510539dup	NC_000006.11:g.21510527_21510539dup	NC_000006.11:g.21510526_21510539dup	NC_000006.11:g.21510525_21510539dup	NC_000006.11:g.21510524_21510539dup	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTT	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTT	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.21510539_21510540insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

77 SubSNP, 51 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95421879	Feb 13, 2009 (130)
2	BILGI_BIOE	ss666345835	Apr 25, 2013 (138)
3	SSIP	ss947164447	Aug 21, 2014 (142)
4	EVA_UK10K_ALSPAC	ss1705072650	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1705072651	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1705072703	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1705072705	Apr 01, 2015 (144)
8	SWEGEN	ss2998639887	Nov 08, 2017 (151)
9	MCHAISSO	ss3064195406	Nov 08, 2017 (151)
10	URBANLAB	ss3648286211	Oct 12, 2018 (152)
11	EVA_DECODE	ss3716737915	Jul 13, 2019 (153)
12	EVA_DECODE	ss3716737916	Jul 13, 2019 (153)
13	EVA_DECODE	ss3716737917	Jul 13, 2019 (153)
14	EVA_DECODE	ss3716737918	Jul 13, 2019 (153)
15	PACBIO	ss3790757049	Jul 13, 2019 (153)
16	PACBIO	ss3790757050	Jul 13, 2019 (153)
17	PACBIO	ss3795634403	Jul 13, 2019 (153)
18	PACBIO	ss3795634404	Jul 13, 2019 (153)
19	EVA	ss3829774684	Apr 26, 2020 (154)
20	KOGIC	ss3958650475	Apr 26, 2020 (154)
21	KOGIC	ss3958650476	Apr 26, 2020 (154)
22	KOGIC	ss3958650477	Apr 26, 2020 (154)
23	KOGIC	ss3958650478	Apr 26, 2020 (154)
24	KOGIC	ss3958650479	Apr 26, 2020 (154)
25	KOGIC	ss3958650480	Apr 26, 2020 (154)
26	GNOMAD	ss4138181088	Apr 26, 2021 (155)
27	GNOMAD	ss4138181089	Apr 26, 2021 (155)
28	GNOMAD	ss4138181090	Apr 26, 2021 (155)
29	GNOMAD	ss4138181091	Apr 26, 2021 (155)
30	GNOMAD	ss4138181092	Apr 26, 2021 (155)
31	GNOMAD	ss4138181093	Apr 26, 2021 (155)
32	GNOMAD	ss4138181094	Apr 26, 2021 (155)
33	GNOMAD	ss4138181095	Apr 26, 2021 (155)
34	GNOMAD	ss4138181096	Apr 26, 2021 (155)
35	GNOMAD	ss4138181097	Apr 26, 2021 (155)
36	GNOMAD	ss4138181098	Apr 26, 2021 (155)
37	GNOMAD	ss4138181099	Apr 26, 2021 (155)
38	GNOMAD	ss4138181100	Apr 26, 2021 (155)
39	GNOMAD	ss4138181101	Apr 26, 2021 (155)
40	GNOMAD	ss4138181102	Apr 26, 2021 (155)
41	GNOMAD	ss4138181103	Apr 26, 2021 (155)
42	GNOMAD	ss4138181104	Apr 26, 2021 (155)
43	GNOMAD	ss4138181105	Apr 26, 2021 (155)
44	GNOMAD	ss4138181106	Apr 26, 2021 (155)
45	GNOMAD	ss4138181107	Apr 26, 2021 (155)
46	GNOMAD	ss4138181108	Apr 26, 2021 (155)
47	GNOMAD	ss4138181109	Apr 26, 2021 (155)
48	GNOMAD	ss4138181110	Apr 26, 2021 (155)
49	GNOMAD	ss4138181112	Apr 26, 2021 (155)
50	GNOMAD	ss4138181113	Apr 26, 2021 (155)
51	GNOMAD	ss4138181114	Apr 26, 2021 (155)
52	GNOMAD	ss4138181115	Apr 26, 2021 (155)
53	GNOMAD	ss4138181116	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5176498045	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5176498046	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5176498047	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5176498048	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5176498049	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5176498050	Apr 26, 2021 (155)
60	1000G_HIGH_COVERAGE	ss5267668258	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5267668259	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5267668260	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5267668261	Oct 13, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5267668262	Oct 13, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5267668263	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5465437247	Oct 13, 2022 (156)
67	HUGCELL_USP	ss5465437248	Oct 13, 2022 (156)
68	HUGCELL_USP	ss5465437249	Oct 13, 2022 (156)
69	HUGCELL_USP	ss5465437250	Oct 13, 2022 (156)
70	HUGCELL_USP	ss5465437251	Oct 13, 2022 (156)
71	HUGCELL_USP	ss5465437252	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5714260511	Oct 13, 2022 (156)
73	TOMMO_GENOMICS	ss5714260512	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5714260513	Oct 13, 2022 (156)
75	TOMMO_GENOMICS	ss5714260514	Oct 13, 2022 (156)
76	TOMMO_GENOMICS	ss5714260515	Oct 13, 2022 (156)
77	TOMMO_GENOMICS	ss5714260516	Oct 13, 2022 (156)
78	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17283985 (NC_000006.11:21510523::TTTTTT 158/3854) Row 17283986 (NC_000006.11:21510523::TTTTTTT 253/3854)	-	Oct 12, 2018 (152)
79	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17283985 (NC_000006.11:21510523::TTTTTT 158/3854) Row 17283986 (NC_000006.11:21510523::TTTTTTT 253/3854)	-	Oct 12, 2018 (152)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 219227158 (NC_000006.12:21510292::T 1989/118736) Row 219227159 (NC_000006.12:21510292::TT 41/118764) Row 219227160 (NC_000006.12:21510292::TTT 1/118762)...	-	Apr 26, 2021 (155)
108	Korean Genome Project Submission ignored due to conflicting rows: Row 15028476 (NC_000006.12:21510292::TTTTTT 363/1828) Row 15028477 (NC_000006.12:21510292::TTTTTTT 1087/1828) Row 15028478 (NC_000006.12:21510292::TTTTTTTT 194/1828)...	-	Apr 26, 2020 (154)
109	Korean Genome Project Submission ignored due to conflicting rows: Row 15028476 (NC_000006.12:21510292::TTTTTT 363/1828) Row 15028477 (NC_000006.12:21510292::TTTTTTT 1087/1828) Row 15028478 (NC_000006.12:21510292::TTTTTTTT 194/1828)...	-	Apr 26, 2020 (154)
110	Korean Genome Project Submission ignored due to conflicting rows: Row 15028476 (NC_000006.12:21510292::TTTTTT 363/1828) Row 15028477 (NC_000006.12:21510292::TTTTTTT 1087/1828) Row 15028478 (NC_000006.12:21510292::TTTTTTTT 194/1828)...	-	Apr 26, 2020 (154)
111	Korean Genome Project Submission ignored due to conflicting rows: Row 15028476 (NC_000006.12:21510292::TTTTTT 363/1828) Row 15028477 (NC_000006.12:21510292::TTTTTTT 1087/1828) Row 15028478 (NC_000006.12:21510292::TTTTTTTT 194/1828)...	-	Apr 26, 2020 (154)
112	Korean Genome Project Submission ignored due to conflicting rows: Row 15028476 (NC_000006.12:21510292::TTTTTT 363/1828) Row 15028477 (NC_000006.12:21510292::TTTTTTT 1087/1828) Row 15028478 (NC_000006.12:21510292::TTTTTTTT 194/1828)...	-	Apr 26, 2020 (154)
113	Korean Genome Project Submission ignored due to conflicting rows: Row 15028476 (NC_000006.12:21510292::TTTTTT 363/1828) Row 15028477 (NC_000006.12:21510292::TTTTTTT 1087/1828) Row 15028478 (NC_000006.12:21510292::TTTTTTTT 194/1828)...	-	Apr 26, 2020 (154)
114	8.3KJPN Submission ignored due to conflicting rows: Row 34467352 (NC_000006.11:21510523::TTTTTTT 14007/16412) Row 34467353 (NC_000006.11:21510523::TTTTTTTT 796/16412) Row 34467354 (NC_000006.11:21510523::TTTTTT 156/16412)...	-	Apr 26, 2021 (155)
115	8.3KJPN Submission ignored due to conflicting rows: Row 34467352 (NC_000006.11:21510523::TTTTTTT 14007/16412) Row 34467353 (NC_000006.11:21510523::TTTTTTTT 796/16412) Row 34467354 (NC_000006.11:21510523::TTTTTT 156/16412)...	-	Apr 26, 2021 (155)
116	8.3KJPN Submission ignored due to conflicting rows: Row 34467352 (NC_000006.11:21510523::TTTTTTT 14007/16412) Row 34467353 (NC_000006.11:21510523::TTTTTTTT 796/16412) Row 34467354 (NC_000006.11:21510523::TTTTTT 156/16412)...	-	Apr 26, 2021 (155)
117	8.3KJPN Submission ignored due to conflicting rows: Row 34467352 (NC_000006.11:21510523::TTTTTTT 14007/16412) Row 34467353 (NC_000006.11:21510523::TTTTTTTT 796/16412) Row 34467354 (NC_000006.11:21510523::TTTTTT 156/16412)...	-	Apr 26, 2021 (155)
118	8.3KJPN Submission ignored due to conflicting rows: Row 34467352 (NC_000006.11:21510523::TTTTTTT 14007/16412) Row 34467353 (NC_000006.11:21510523::TTTTTTTT 796/16412) Row 34467354 (NC_000006.11:21510523::TTTTTT 156/16412)...	-	Apr 26, 2021 (155)
119	8.3KJPN Submission ignored due to conflicting rows: Row 34467352 (NC_000006.11:21510523::TTTTTTT 14007/16412) Row 34467353 (NC_000006.11:21510523::TTTTTTTT 796/16412) Row 34467354 (NC_000006.11:21510523::TTTTTT 156/16412)...	-	Apr 26, 2021 (155)
120	14KJPN Submission ignored due to conflicting rows: Row 48097615 (NC_000006.12:21510292::TTTTTTT 23834/27930) Row 48097616 (NC_000006.12:21510292::TTTTTT 183/27930) Row 48097617 (NC_000006.12:21510292::TTTTTTTT 1240/27930)...	-	Oct 13, 2022 (156)
121	14KJPN Submission ignored due to conflicting rows: Row 48097615 (NC_000006.12:21510292::TTTTTTT 23834/27930) Row 48097616 (NC_000006.12:21510292::TTTTTT 183/27930) Row 48097617 (NC_000006.12:21510292::TTTTTTTT 1240/27930)...	-	Oct 13, 2022 (156)
122	14KJPN Submission ignored due to conflicting rows: Row 48097615 (NC_000006.12:21510292::TTTTTTT 23834/27930) Row 48097616 (NC_000006.12:21510292::TTTTTT 183/27930) Row 48097617 (NC_000006.12:21510292::TTTTTTTT 1240/27930)...	-	Oct 13, 2022 (156)
123	14KJPN Submission ignored due to conflicting rows: Row 48097615 (NC_000006.12:21510292::TTTTTTT 23834/27930) Row 48097616 (NC_000006.12:21510292::TTTTTT 183/27930) Row 48097617 (NC_000006.12:21510292::TTTTTTTT 1240/27930)...	-	Oct 13, 2022 (156)
124	14KJPN Submission ignored due to conflicting rows: Row 48097615 (NC_000006.12:21510292::TTTTTTT 23834/27930) Row 48097616 (NC_000006.12:21510292::TTTTTT 183/27930) Row 48097617 (NC_000006.12:21510292::TTTTTTTT 1240/27930)...	-	Oct 13, 2022 (156)
125	14KJPN Submission ignored due to conflicting rows: Row 48097615 (NC_000006.12:21510292::TTTTTTT 23834/27930) Row 48097616 (NC_000006.12:21510292::TTTTTT 183/27930) Row 48097617 (NC_000006.12:21510292::TTTTTTTT 1240/27930)...	-	Oct 13, 2022 (156)
126	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17283985 (NC_000006.11:21510523::TTTTTT 149/3708) Row 17283986 (NC_000006.11:21510523::TTTTTTT 274/3708)	-	Oct 12, 2018 (152)
127	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17283985 (NC_000006.11:21510523::TTTTTT 149/3708) Row 17283986 (NC_000006.11:21510523::TTTTTTT 274/3708)	-	Oct 12, 2018 (152)
128	ALFA	NC_000006.12 - 21510293	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
ss4138181116	NC_000006.12:21510292:TTTTT:	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4138181115	NC_000006.12:21510292:TTTT:	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4138181114	NC_000006.12:21510292:TTT:	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4138181113	NC_000006.12:21510292:TT:	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss2998639887	NC_000006.11:21510523:T:	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3716737915, ss4138181112, ss5267668263, ss5465437250	NC_000006.12:21510292:T:	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4138181088, ss5267668259, ss5465437249	NC_000006.12:21510292::T	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4138181089	NC_000006.12:21510292::TT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4138181090	NC_000006.12:21510292::TTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5176498049	NC_000006.11:21510523::TTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4138181091, ss5714260515	NC_000006.12:21510292::TTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3958650478, ss4138181092	NC_000006.12:21510292::TTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3716737916	NC_000006.12:21510293::TTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1705072650, ss1705072703, ss3790757049, ss3795634403, ss5176498047	NC_000006.11:21510523::TTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3958650475, ss4138181093, ss5267668261, ss5465437247, ss5714260512	NC_000006.12:21510292::TTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3716737917	NC_000006.12:21510293::TTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss666345835, ss1705072651, ss1705072705, ss3790757050, ss3795634404, ss3829774684, ss5176498045	NC_000006.11:21510523::TTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss947164447	NC_000006.11:21510524::TTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3064195406, ss3958650476, ss4138181094, ss5267668258, ss5465437248, ss5714260511	NC_000006.12:21510292::TTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3716737918	NC_000006.12:21510293::TTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95421879	NT_007592.15:21450539::TTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5176498046	NC_000006.11:21510523::TTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3648286211, ss3958650477, ss4138181095, ss5267668260, ss5465437251, ss5714260513	NC_000006.12:21510292::TTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5176498048	NC_000006.11:21510523::TTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3958650480, ss4138181096, ss5267668262, ss5714260514	NC_000006.12:21510292::TTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181097	NC_000006.12:21510292::TTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181098	NC_000006.12:21510292::TTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181099	NC_000006.12:21510292::TTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181100	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181101	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181102	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5176498050	NC_000006.11:21510523::TTTTTTTTTTT… NC_000006.11:21510523::TTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3958650479, ss4138181103, ss5465437252, ss5714260516	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10939035057	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181104	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181105	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181106	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181107	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181108	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181109	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138181110	NC_000006.12:21510292::TTTTTTTTTTT… NC_000006.12:21510292::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:21510292:TTTTTTTTTTTT… NC_000006.12:21510292:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs70993246

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs70993246