Name: rs71106683
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.

rs71106683

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:102463323-102463347 (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)₁₇ / del(T)₁₄ / del(T)₁₃ / d…
del(T)₁₇ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₃ / dup(T)₁₉ / dup(T)₂₁ / ins(T)₃₃
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1601 (940/5870, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ALKBH4 : Intron Variant
LRWD1 : 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	5870	TTTTTTTTTTTTTTTTTTTTTTTTT=0.6951	TTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0523, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1601, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0349, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0097, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0458, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0020	0.833333	0.125443	0.041223	32
European	Sub	4926	TTTTTTTTTTTTTTTTTTTTTTTTT=0.6378	TTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0621, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1904, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0410, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0116, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0546, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0024	0.789591	0.158366	0.052043	32
African	Sub	718	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	692	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	30	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	104	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	70	TTTTTTTTTTTTTTTTTTTTTTTTT=0.91	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5870	(T)₂₅=0.6951	del(T)₁₇=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0523, dupT=0.1601, dupTT=0.0458, dupTTT=0.0349, dup(T)₄=0.0097, ins(T)₃₃=0.0020
Allele Frequency Aggregator	European	Sub	4926	(T)₂₅=0.6378	del(T)₁₇=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0621, dupT=0.1904, dupTT=0.0546, dupTTT=0.0410, dup(T)₄=0.0116, ins(T)₃₃=0.0024
Allele Frequency Aggregator	African	Sub	718	(T)₂₅=1.000	del(T)₁₇=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, 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, dupTTT=0.000, dup(T)₄=0.000, ins(T)₃₃=0.000
Allele Frequency Aggregator	Latin American 2	Sub	104	(T)₂₅=1.000	del(T)₁₇=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, 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, dupTTT=0.000, dup(T)₄=0.000, ins(T)₃₃=0.000
Allele Frequency Aggregator	Other	Sub	70	(T)₂₅=0.91	del(T)₁₇=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.01, dupT=0.03, dupTT=0.00, dupTTT=0.04, dup(T)₄=0.00, ins(T)₃₃=0.00
Allele Frequency Aggregator	Asian	Sub	30	(T)₂₅=1.00	del(T)₁₇=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, 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, dupTTT=0.00, dup(T)₄=0.00, ins(T)₃₃=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₂₅=1.00	del(T)₁₇=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, 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, dupTTT=0.00, dup(T)₄=0.00, ins(T)₃₃=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(T)₂₅=1.0	del(T)₁₇=0.0, del(T)₁₄=0.0, del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, 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, dupTTT=0.0, dup(T)₄=0.0, ins(T)₃₃=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 7	NC_000007.14:g.102463331_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463334_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463335_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463336_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463337_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463338_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463339_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463340_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463341_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463342_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463343_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463344_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463345_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463346_102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463347del
GRCh38.p14 chr 7	NC_000007.14:g.102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463346_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463345_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463344_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463343_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463342_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463341_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463340_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463339_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463335_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463329_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463327_102463347dup
GRCh38.p14 chr 7	NC_000007.14:g.102463347_102463348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.102103778_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103781_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103782_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103783_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103784_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103785_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103786_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103787_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103788_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103789_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103790_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103791_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103792_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103793_102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103794del
GRCh37.p13 chr 7	NC_000007.13:g.102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103793_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103792_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103791_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103790_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103789_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103788_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103787_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103786_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103782_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103776_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103774_102103794dup
GRCh37.p13 chr 7	NC_000007.13:g.102103794_102103795insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: ALKBH4, alkB homolog 4, lysine demethylase (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ALKBH4 transcript	NM_017621.4:c.123+1375_12… NM_017621.4:c.123+1375_123+1391del	N/A	Intron Variant
ALKBH4 transcript variant X1	XM_005250464.4:c.-6+1375_… XM_005250464.4:c.-6+1375_-6+1391del	N/A	Intron Variant

Gene: LRWD1, leucine rich repeats and WD repeat domain containing 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LRWD1 transcript variant 2	NM_001317721.2:c.	N/A	Upstream Transcript Variant
LRWD1 transcript variant 1	NM_152892.3:c.	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	(T)₂₅=	del(T)₁₇	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₃	dup(T)₁₉	dup(T)₂₁	ins(T)₃₃
GRCh38.p14 chr 7	NC_000007.14:g.102463323_102463347=	NC_000007.14:g.102463331_102463347del	NC_000007.14:g.102463334_102463347del	NC_000007.14:g.102463335_102463347del	NC_000007.14:g.102463336_102463347del	NC_000007.14:g.102463337_102463347del	NC_000007.14:g.102463338_102463347del	NC_000007.14:g.102463339_102463347del	NC_000007.14:g.102463340_102463347del	NC_000007.14:g.102463341_102463347del	NC_000007.14:g.102463342_102463347del	NC_000007.14:g.102463343_102463347del	NC_000007.14:g.102463344_102463347del	NC_000007.14:g.102463345_102463347del	NC_000007.14:g.102463346_102463347del	NC_000007.14:g.102463347del	NC_000007.14:g.102463347dup	NC_000007.14:g.102463346_102463347dup	NC_000007.14:g.102463345_102463347dup	NC_000007.14:g.102463344_102463347dup	NC_000007.14:g.102463343_102463347dup	NC_000007.14:g.102463342_102463347dup	NC_000007.14:g.102463341_102463347dup	NC_000007.14:g.102463340_102463347dup	NC_000007.14:g.102463339_102463347dup	NC_000007.14:g.102463335_102463347dup	NC_000007.14:g.102463329_102463347dup	NC_000007.14:g.102463327_102463347dup	NC_000007.14:g.102463347_102463348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.102103770_102103794=	NC_000007.13:g.102103778_102103794del	NC_000007.13:g.102103781_102103794del	NC_000007.13:g.102103782_102103794del	NC_000007.13:g.102103783_102103794del	NC_000007.13:g.102103784_102103794del	NC_000007.13:g.102103785_102103794del	NC_000007.13:g.102103786_102103794del	NC_000007.13:g.102103787_102103794del	NC_000007.13:g.102103788_102103794del	NC_000007.13:g.102103789_102103794del	NC_000007.13:g.102103790_102103794del	NC_000007.13:g.102103791_102103794del	NC_000007.13:g.102103792_102103794del	NC_000007.13:g.102103793_102103794del	NC_000007.13:g.102103794del	NC_000007.13:g.102103794dup	NC_000007.13:g.102103793_102103794dup	NC_000007.13:g.102103792_102103794dup	NC_000007.13:g.102103791_102103794dup	NC_000007.13:g.102103790_102103794dup	NC_000007.13:g.102103789_102103794dup	NC_000007.13:g.102103788_102103794dup	NC_000007.13:g.102103787_102103794dup	NC_000007.13:g.102103786_102103794dup	NC_000007.13:g.102103782_102103794dup	NC_000007.13:g.102103776_102103794dup	NC_000007.13:g.102103774_102103794dup	NC_000007.13:g.102103794_102103795insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ALKBH4 transcript	NM_017621.3:c.123+1391=	NM_017621.3:c.123+1375_123+1391del	NM_017621.3:c.123+1378_123+1391del	NM_017621.3:c.123+1379_123+1391del	NM_017621.3:c.123+1380_123+1391del	NM_017621.3:c.123+1381_123+1391del	NM_017621.3:c.123+1382_123+1391del	NM_017621.3:c.123+1383_123+1391del	NM_017621.3:c.123+1384_123+1391del	NM_017621.3:c.123+1385_123+1391del	NM_017621.3:c.123+1386_123+1391del	NM_017621.3:c.123+1387_123+1391del	NM_017621.3:c.123+1388_123+1391del	NM_017621.3:c.123+1389_123+1391del	NM_017621.3:c.123+1390_123+1391del	NM_017621.3:c.123+1391del	NM_017621.3:c.123+1391dup	NM_017621.3:c.123+1390_123+1391dup	NM_017621.3:c.123+1389_123+1391dup	NM_017621.3:c.123+1388_123+1391dup	NM_017621.3:c.123+1387_123+1391dup	NM_017621.3:c.123+1386_123+1391dup	NM_017621.3:c.123+1385_123+1391dup	NM_017621.3:c.123+1384_123+1391dup	NM_017621.3:c.123+1383_123+1391dup	NM_017621.3:c.123+1379_123+1391dup	NM_017621.3:c.123+1373_123+1391dup	NM_017621.3:c.123+1371_123+1391dup	NM_017621.3:c.123+1391_123+1392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ALKBH4 transcript	NM_017621.4:c.123+1391=	NM_017621.4:c.123+1375_123+1391del	NM_017621.4:c.123+1378_123+1391del	NM_017621.4:c.123+1379_123+1391del	NM_017621.4:c.123+1380_123+1391del	NM_017621.4:c.123+1381_123+1391del	NM_017621.4:c.123+1382_123+1391del	NM_017621.4:c.123+1383_123+1391del	NM_017621.4:c.123+1384_123+1391del	NM_017621.4:c.123+1385_123+1391del	NM_017621.4:c.123+1386_123+1391del	NM_017621.4:c.123+1387_123+1391del	NM_017621.4:c.123+1388_123+1391del	NM_017621.4:c.123+1389_123+1391del	NM_017621.4:c.123+1390_123+1391del	NM_017621.4:c.123+1391del	NM_017621.4:c.123+1391dup	NM_017621.4:c.123+1390_123+1391dup	NM_017621.4:c.123+1389_123+1391dup	NM_017621.4:c.123+1388_123+1391dup	NM_017621.4:c.123+1387_123+1391dup	NM_017621.4:c.123+1386_123+1391dup	NM_017621.4:c.123+1385_123+1391dup	NM_017621.4:c.123+1384_123+1391dup	NM_017621.4:c.123+1383_123+1391dup	NM_017621.4:c.123+1379_123+1391dup	NM_017621.4:c.123+1373_123+1391dup	NM_017621.4:c.123+1371_123+1391dup	NM_017621.4:c.123+1391_123+1392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ALKBH4 transcript variant X1	XM_005250464.1:c.-6+1391=	XM_005250464.1:c.-6+1375_-6+1391del	XM_005250464.1:c.-6+1378_-6+1391del	XM_005250464.1:c.-6+1379_-6+1391del	XM_005250464.1:c.-6+1380_-6+1391del	XM_005250464.1:c.-6+1381_-6+1391del	XM_005250464.1:c.-6+1382_-6+1391del	XM_005250464.1:c.-6+1383_-6+1391del	XM_005250464.1:c.-6+1384_-6+1391del	XM_005250464.1:c.-6+1385_-6+1391del	XM_005250464.1:c.-6+1386_-6+1391del	XM_005250464.1:c.-6+1387_-6+1391del	XM_005250464.1:c.-6+1388_-6+1391del	XM_005250464.1:c.-6+1389_-6+1391del	XM_005250464.1:c.-6+1390_-6+1391del	XM_005250464.1:c.-6+1391del	XM_005250464.1:c.-6+1391dup	XM_005250464.1:c.-6+1390_-6+1391dup	XM_005250464.1:c.-6+1389_-6+1391dup	XM_005250464.1:c.-6+1388_-6+1391dup	XM_005250464.1:c.-6+1387_-6+1391dup	XM_005250464.1:c.-6+1386_-6+1391dup	XM_005250464.1:c.-6+1385_-6+1391dup	XM_005250464.1:c.-6+1384_-6+1391dup	XM_005250464.1:c.-6+1383_-6+1391dup	XM_005250464.1:c.-6+1379_-6+1391dup	XM_005250464.1:c.-6+1373_-6+1391dup	XM_005250464.1:c.-6+1371_-6+1391dup	XM_005250464.1:c.-6+1391_-6+1392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ALKBH4 transcript variant X1	XM_005250464.4:c.-6+1391=	XM_005250464.4:c.-6+1375_-6+1391del	XM_005250464.4:c.-6+1378_-6+1391del	XM_005250464.4:c.-6+1379_-6+1391del	XM_005250464.4:c.-6+1380_-6+1391del	XM_005250464.4:c.-6+1381_-6+1391del	XM_005250464.4:c.-6+1382_-6+1391del	XM_005250464.4:c.-6+1383_-6+1391del	XM_005250464.4:c.-6+1384_-6+1391del	XM_005250464.4:c.-6+1385_-6+1391del	XM_005250464.4:c.-6+1386_-6+1391del	XM_005250464.4:c.-6+1387_-6+1391del	XM_005250464.4:c.-6+1388_-6+1391del	XM_005250464.4:c.-6+1389_-6+1391del	XM_005250464.4:c.-6+1390_-6+1391del	XM_005250464.4:c.-6+1391del	XM_005250464.4:c.-6+1391dup	XM_005250464.4:c.-6+1390_-6+1391dup	XM_005250464.4:c.-6+1389_-6+1391dup	XM_005250464.4:c.-6+1388_-6+1391dup	XM_005250464.4:c.-6+1387_-6+1391dup	XM_005250464.4:c.-6+1386_-6+1391dup	XM_005250464.4:c.-6+1385_-6+1391dup	XM_005250464.4:c.-6+1384_-6+1391dup	XM_005250464.4:c.-6+1383_-6+1391dup	XM_005250464.4:c.-6+1379_-6+1391dup	XM_005250464.4:c.-6+1373_-6+1391dup	XM_005250464.4:c.-6+1371_-6+1391dup	XM_005250464.4:c.-6+1391_-6+1392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ALKBH4 transcript variant X2	XM_005250465.1:c.-288+1391=	XM_005250465.1:c.-288+1375_-288+1391del	XM_005250465.1:c.-288+1378_-288+1391del	XM_005250465.1:c.-288+1379_-288+1391del	XM_005250465.1:c.-288+1380_-288+1391del	XM_005250465.1:c.-288+1381_-288+1391del	XM_005250465.1:c.-288+1382_-288+1391del	XM_005250465.1:c.-288+1383_-288+1391del	XM_005250465.1:c.-288+1384_-288+1391del	XM_005250465.1:c.-288+1385_-288+1391del	XM_005250465.1:c.-288+1386_-288+1391del	XM_005250465.1:c.-288+1387_-288+1391del	XM_005250465.1:c.-288+1388_-288+1391del	XM_005250465.1:c.-288+1389_-288+1391del	XM_005250465.1:c.-288+1390_-288+1391del	XM_005250465.1:c.-288+1391del	XM_005250465.1:c.-288+1391dup	XM_005250465.1:c.-288+1390_-288+1391dup	XM_005250465.1:c.-288+1389_-288+1391dup	XM_005250465.1:c.-288+1388_-288+1391dup	XM_005250465.1:c.-288+1387_-288+1391dup	XM_005250465.1:c.-288+1386_-288+1391dup	XM_005250465.1:c.-288+1385_-288+1391dup	XM_005250465.1:c.-288+1384_-288+1391dup	XM_005250465.1:c.-288+1383_-288+1391dup	XM_005250465.1:c.-288+1379_-288+1391dup	XM_005250465.1:c.-288+1373_-288+1391dup	XM_005250465.1:c.-288+1371_-288+1391dup	XM_005250465.1:c.-288+1391_-288+1392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

53 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95470159	Feb 13, 2009 (130)
2	BCMHGSC_JDW	ss103755437	Mar 15, 2016 (147)
3	PJP	ss295349046	May 09, 2011 (137)
4	EVA_UK10K_ALSPAC	ss1705757553	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1705757554	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1705757712	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1705757716	Apr 01, 2015 (144)
8	SWEGEN	ss3001744392	Nov 08, 2017 (151)
9	EVA	ss3830732260	Apr 26, 2020 (154)
10	GNOMAD	ss4169794658	Apr 26, 2021 (155)
11	GNOMAD	ss4169794659	Apr 26, 2021 (155)
12	GNOMAD	ss4169794660	Apr 26, 2021 (155)
13	GNOMAD	ss4169794661	Apr 26, 2021 (155)
14	GNOMAD	ss4169794662	Apr 26, 2021 (155)
15	GNOMAD	ss4169794663	Apr 26, 2021 (155)
16	GNOMAD	ss4169794664	Apr 26, 2021 (155)
17	GNOMAD	ss4169794665	Apr 26, 2021 (155)
18	GNOMAD	ss4169794666	Apr 26, 2021 (155)
19	GNOMAD	ss4169794667	Apr 26, 2021 (155)
20	GNOMAD	ss4169794668	Apr 26, 2021 (155)
21	GNOMAD	ss4169794669	Apr 26, 2021 (155)
22	GNOMAD	ss4169794671	Apr 26, 2021 (155)
23	GNOMAD	ss4169794672	Apr 26, 2021 (155)
24	GNOMAD	ss4169794673	Apr 26, 2021 (155)
25	GNOMAD	ss4169794674	Apr 26, 2021 (155)
26	GNOMAD	ss4169794675	Apr 26, 2021 (155)
27	GNOMAD	ss4169794676	Apr 26, 2021 (155)
28	GNOMAD	ss4169794677	Apr 26, 2021 (155)
29	GNOMAD	ss4169794678	Apr 26, 2021 (155)
30	GNOMAD	ss4169794679	Apr 26, 2021 (155)
31	GNOMAD	ss4169794680	Apr 26, 2021 (155)
32	GNOMAD	ss4169794681	Apr 26, 2021 (155)
33	GNOMAD	ss4169794682	Apr 26, 2021 (155)
34	GNOMAD	ss4169794683	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5184765177	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5184765178	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5184765179	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5184765180	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5184765181	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5184765182	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5274107428	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5274107429	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5274107430	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5274107431	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5274107432	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5471066115	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5471066116	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5725518090	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5725518091	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5725518092	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5725518093	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5725518094	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5725518095	Oct 16, 2022 (156)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 21382519 (NC_000007.13:102103769::TT 2432/3854) Row 21382520 (NC_000007.13:102103769::TTT 1395/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 21382519 (NC_000007.13:102103769::TT 2432/3854) Row 21382520 (NC_000007.13:102103769::TTT 1395/3854)	-	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271250807 (NC_000007.14:102463322::T 27503/55638) Row 271250808 (NC_000007.14:102463322::TT 4996/55408) Row 271250809 (NC_000007.14:102463322::TTT 3484/55318)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 42734484 (NC_000007.13:102103769::T 3530/15992) Row 42734485 (NC_000007.13:102103769:TTTTTTTTTTTTT: 15/15992) Row 42734486 (NC_000007.13:102103769::TT 135/15992)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 42734484 (NC_000007.13:102103769::T 3530/15992) Row 42734485 (NC_000007.13:102103769:TTTTTTTTTTTTT: 15/15992) Row 42734486 (NC_000007.13:102103769::TT 135/15992)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 42734484 (NC_000007.13:102103769::T 3530/15992) Row 42734485 (NC_000007.13:102103769:TTTTTTTTTTTTT: 15/15992) Row 42734486 (NC_000007.13:102103769::TT 135/15992)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 42734484 (NC_000007.13:102103769::T 3530/15992) Row 42734485 (NC_000007.13:102103769:TTTTTTTTTTTTT: 15/15992) Row 42734486 (NC_000007.13:102103769::TT 135/15992)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 42734484 (NC_000007.13:102103769::T 3530/15992) Row 42734485 (NC_000007.13:102103769:TTTTTTTTTTTTT: 15/15992) Row 42734486 (NC_000007.13:102103769::TT 135/15992)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 42734484 (NC_000007.13:102103769::T 3530/15992) Row 42734485 (NC_000007.13:102103769:TTTTTTTTTTTTT: 15/15992) Row 42734486 (NC_000007.13:102103769::TT 135/15992)...	-	Apr 26, 2021 (155)
87	14KJPN Submission ignored due to conflicting rows: Row 59355194 (NC_000007.14:102463322::T 5794/26574) Row 59355195 (NC_000007.14:102463322::TT 151/26574) Row 59355196 (NC_000007.14:102463322:TTTTTTTTTTTTT: 27/26574)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 59355194 (NC_000007.14:102463322::T 5794/26574) Row 59355195 (NC_000007.14:102463322::TT 151/26574) Row 59355196 (NC_000007.14:102463322:TTTTTTTTTTTTT: 27/26574)...	-	Oct 16, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 59355194 (NC_000007.14:102463322::T 5794/26574) Row 59355195 (NC_000007.14:102463322::TT 151/26574) Row 59355196 (NC_000007.14:102463322:TTTTTTTTTTTTT: 27/26574)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 59355194 (NC_000007.14:102463322::T 5794/26574) Row 59355195 (NC_000007.14:102463322::TT 151/26574) Row 59355196 (NC_000007.14:102463322:TTTTTTTTTTTTT: 27/26574)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 59355194 (NC_000007.14:102463322::T 5794/26574) Row 59355195 (NC_000007.14:102463322::TT 151/26574) Row 59355196 (NC_000007.14:102463322:TTTTTTTTTTTTT: 27/26574)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 59355194 (NC_000007.14:102463322::T 5794/26574) Row 59355195 (NC_000007.14:102463322::TT 151/26574) Row 59355196 (NC_000007.14:102463322:TTTTTTTTTTTTT: 27/26574)...	-	Oct 16, 2022 (156)
93	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21382519 (NC_000007.13:102103769::TT 2284/3708) Row 21382520 (NC_000007.13:102103769::TTT 1394/3708)	-	Oct 12, 2018 (152)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21382519 (NC_000007.13:102103769::TT 2284/3708) Row 21382520 (NC_000007.13:102103769::TTT 1394/3708)	-	Oct 12, 2018 (152)
95	ALFA	NC_000007.14 - 102463323	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).

Associated ID	History Updated (Build)
rs139854555	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3001744392	NC_000007.13:102103769:TTTTTTTTTTT… NC_000007.13:102103769:TTTTTTTTTTTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4169794683, ss5274107432	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5184765178	NC_000007.13:102103769:TTTTTTTTTTT… NC_000007.13:102103769:TTTTTTTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4169794682, ss5725518092	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4169794681	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4169794680	NC_000007.14:102463322:TTTTTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4169794679	NC_000007.14:102463322:TTTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4169794678	NC_000007.14:102463322:TTTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5184765182	NC_000007.13:102103769:TTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4169794677	NC_000007.14:102463322:TTTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4169794676	NC_000007.14:102463322:TTTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4169794675	NC_000007.14:102463322:TTTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4169794674	NC_000007.14:102463322:TTTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794673	NC_000007.14:102463322:TTT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794672, ss5274107431, ss5725518095	NC_000007.14:102463322:TT:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5184765180	NC_000007.13:102103769:T:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794671, ss5274107430, ss5471066116, ss5725518093	NC_000007.14:102463322:T:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103755437	NT_007933.15:40136614:T:	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295349046	NC_000007.12:101890775::T	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3830732260, ss5184765177	NC_000007.13:102103769::T	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794658, ss5471066115, ss5725518090	NC_000007.14:102463322::T	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95470159	NT_007933.15:40136637::T	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1705757553, ss1705757712, ss5184765179	NC_000007.13:102103769::TT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794659, ss5274107428, ss5725518091	NC_000007.14:102463322::TT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1705757554, ss1705757716, ss5184765181	NC_000007.13:102103769::TTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794660, ss5274107429, ss5725518094	NC_000007.14:102463322::TTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794661	NC_000007.14:102463322::TTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794662	NC_000007.14:102463322::TTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794663	NC_000007.14:102463322::TTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794664	NC_000007.14:102463322::TTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794665	NC_000007.14:102463322::TTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794666	NC_000007.14:102463322::TTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794667	NC_000007.14:102463322::TTTTTTTTTT… NC_000007.14:102463322::TTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794668	NC_000007.14:102463322::TTTTTTTTTT… NC_000007.14:102463322::TTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169794669	NC_000007.14:102463322::TTTTTTTTTT… NC_000007.14:102463322::TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9355858430	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:102463322:TTTTTTTTTTT… NC_000007.14:102463322:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs71106683

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

rs71106683