Name: rs35575527
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.

rs35575527

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:64695604-64695629 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / d…
del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: (T)₂₆=0.3606 (1806/5008, 1000G)
delTT=0.1878 (914/4866, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP7B1 : 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	4866	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.6274	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0253, TTTTTTTTTTTTTTTTTT=0.0053, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0884, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0242, TTTTTTTTTTTTTTTTTTTTTTTT=0.1878, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0415, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.774956	0.12404	0.101004	32
European	Sub	4772	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.6209	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0258, TTTTTTTTTTTTTTTTTT=0.0054, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0899, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0247, TTTTTTTTTTTTTTTTTTTTTTTT=0.1909, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0423, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.769277	0.126897	0.103825	32
African	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	26	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.85	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=0.04, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.12, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.916667	0.083333	0.0	7

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
1000Genomes	Global	Study-wide	5008	(T)₂₆=0.3606	del(T)₉=0.6394
1000Genomes	African	Sub	1322	(T)₂₆=0.2050	del(T)₉=0.7950
1000Genomes	East Asian	Sub	1008	(T)₂₆=0.5536	del(T)₉=0.4464
1000Genomes	Europe	Sub	1006	(T)₂₆=0.2475	del(T)₉=0.7525
1000Genomes	South Asian	Sub	978	(T)₂₆=0.453	del(T)₉=0.547
1000Genomes	American	Sub	694	(T)₂₆=0.411	del(T)₉=0.589
Allele Frequency Aggregator	Total	Global	4866	(T)₂₆=0.6274	del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0253, del(T)₈=0.0053, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0884, del(T)₄=0.0000, delTTT=0.0242, delTT=0.1878, delT=0.0415, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	4772	(T)₂₆=0.6209	del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0258, del(T)₈=0.0054, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0899, del(T)₄=0.0000, delTTT=0.0247, delTT=0.1909, delT=0.0423, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Other	Sub	26	(T)₂₆=0.85	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.04, del(T)₄=0.00, delTTT=0.00, delTT=0.12, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	African	Sub	22	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)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
Allele Frequency Aggregator	Latin American 2	Sub	18	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)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
Allele Frequency Aggregator	Asian	Sub	16	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)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
Allele Frequency Aggregator	South Asian	Sub	12	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)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
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₆=0	del(T)₁₅=0, del(T)₁₄=0, del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=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 8	NC_000008.11:g.64695615_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695616_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695617_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695618_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695619_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695620_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695621_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695622_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695623_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695624_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695625_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695626_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695627_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695628_64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695629del
GRCh38.p14 chr 8	NC_000008.11:g.64695629dup
GRCh38.p14 chr 8	NC_000008.11:g.64695628_64695629dup
GRCh38.p14 chr 8	NC_000008.11:g.64695627_64695629dup
GRCh38.p14 chr 8	NC_000008.11:g.64695626_64695629dup
GRCh37.p13 chr 8	NC_000008.10:g.65608172_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608173_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608174_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608175_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608176_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608177_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608178_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608179_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608180_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608181_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608182_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608183_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608184_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608185_65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608186del
GRCh37.p13 chr 8	NC_000008.10:g.65608186dup
GRCh37.p13 chr 8	NC_000008.10:g.65608185_65608186dup
GRCh37.p13 chr 8	NC_000008.10:g.65608184_65608186dup
GRCh37.p13 chr 8	NC_000008.10:g.65608183_65608186dup
CYP7B1 RefSeqGene	NG_008338.2:g.108174_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108175_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108176_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108177_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108178_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108179_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108180_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108181_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108182_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108183_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108184_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108185_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108186_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108187_108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108188del
CYP7B1 RefSeqGene	NG_008338.2:g.108188dup
CYP7B1 RefSeqGene	NG_008338.2:g.108187_108188dup
CYP7B1 RefSeqGene	NG_008338.2:g.108186_108188dup
CYP7B1 RefSeqGene	NG_008338.2:g.108185_108188dup

Gene: CYP7B1, cytochrome P450 family 7 subfamily B member 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CYP7B1 transcript variant 2	NM_001324112.2:c.123-7107… NM_001324112.2:c.123-71079_123-71065del	N/A	Intron Variant
CYP7B1 transcript variant 1	NM_004820.5:c.123-71079_1… NM_004820.5:c.123-71079_123-71065del	N/A	Intron Variant
CYP7B1 transcript variant X1	XM_017014002.2:c.-3424_-3… XM_017014002.2:c.-3424_-3399=	N/A	5 Prime UTR Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₆=	del(T)₁₅	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 8	NC_000008.11:g.64695604_64695629=	NC_000008.11:g.64695615_64695629del	NC_000008.11:g.64695616_64695629del	NC_000008.11:g.64695617_64695629del	NC_000008.11:g.64695618_64695629del	NC_000008.11:g.64695619_64695629del	NC_000008.11:g.64695620_64695629del	NC_000008.11:g.64695621_64695629del	NC_000008.11:g.64695622_64695629del	NC_000008.11:g.64695623_64695629del	NC_000008.11:g.64695624_64695629del	NC_000008.11:g.64695625_64695629del	NC_000008.11:g.64695626_64695629del	NC_000008.11:g.64695627_64695629del	NC_000008.11:g.64695628_64695629del	NC_000008.11:g.64695629del	NC_000008.11:g.64695629dup	NC_000008.11:g.64695628_64695629dup	NC_000008.11:g.64695627_64695629dup	NC_000008.11:g.64695626_64695629dup
GRCh37.p13 chr 8	NC_000008.10:g.65608161_65608186=	NC_000008.10:g.65608172_65608186del	NC_000008.10:g.65608173_65608186del	NC_000008.10:g.65608174_65608186del	NC_000008.10:g.65608175_65608186del	NC_000008.10:g.65608176_65608186del	NC_000008.10:g.65608177_65608186del	NC_000008.10:g.65608178_65608186del	NC_000008.10:g.65608179_65608186del	NC_000008.10:g.65608180_65608186del	NC_000008.10:g.65608181_65608186del	NC_000008.10:g.65608182_65608186del	NC_000008.10:g.65608183_65608186del	NC_000008.10:g.65608184_65608186del	NC_000008.10:g.65608185_65608186del	NC_000008.10:g.65608186del	NC_000008.10:g.65608186dup	NC_000008.10:g.65608185_65608186dup	NC_000008.10:g.65608184_65608186dup	NC_000008.10:g.65608183_65608186dup
CYP7B1 RefSeqGene	NG_008338.2:g.108163_108188=	NG_008338.2:g.108174_108188del	NG_008338.2:g.108175_108188del	NG_008338.2:g.108176_108188del	NG_008338.2:g.108177_108188del	NG_008338.2:g.108178_108188del	NG_008338.2:g.108179_108188del	NG_008338.2:g.108180_108188del	NG_008338.2:g.108181_108188del	NG_008338.2:g.108182_108188del	NG_008338.2:g.108183_108188del	NG_008338.2:g.108184_108188del	NG_008338.2:g.108185_108188del	NG_008338.2:g.108186_108188del	NG_008338.2:g.108187_108188del	NG_008338.2:g.108188del	NG_008338.2:g.108188dup	NG_008338.2:g.108187_108188dup	NG_008338.2:g.108186_108188dup	NG_008338.2:g.108185_108188dup
CYP7B1 transcript variant X1	XM_017014002.2:c.-3424_-3399=	XM_017014002.2:c.-3413_-3399del	XM_017014002.2:c.-3412_-3399del	XM_017014002.2:c.-3411_-3399del	XM_017014002.2:c.-3410_-3399del	XM_017014002.2:c.-3409_-3399del	XM_017014002.2:c.-3408_-3399del	XM_017014002.2:c.-3407_-3399del	XM_017014002.2:c.-3406_-3399del	XM_017014002.2:c.-3405_-3399del	XM_017014002.2:c.-3404_-3399del	XM_017014002.2:c.-3403_-3399del	XM_017014002.2:c.-3402_-3399del	XM_017014002.2:c.-3401_-3399del	XM_017014002.2:c.-3400_-3399del	XM_017014002.2:c.-3399del	XM_017014002.2:c.-3399dup	XM_017014002.2:c.-3400_-3399dup	XM_017014002.2:c.-3401_-3399dup	XM_017014002.2:c.-3402_-3399dup
CYP7B1 transcript variant X1	XM_017014002.1:c.-3424_-3399=	XM_017014002.1:c.-3413_-3399del	XM_017014002.1:c.-3412_-3399del	XM_017014002.1:c.-3411_-3399del	XM_017014002.1:c.-3410_-3399del	XM_017014002.1:c.-3409_-3399del	XM_017014002.1:c.-3408_-3399del	XM_017014002.1:c.-3407_-3399del	XM_017014002.1:c.-3406_-3399del	XM_017014002.1:c.-3405_-3399del	XM_017014002.1:c.-3404_-3399del	XM_017014002.1:c.-3403_-3399del	XM_017014002.1:c.-3402_-3399del	XM_017014002.1:c.-3401_-3399del	XM_017014002.1:c.-3400_-3399del	XM_017014002.1:c.-3399del	XM_017014002.1:c.-3399dup	XM_017014002.1:c.-3400_-3399dup	XM_017014002.1:c.-3401_-3399dup	XM_017014002.1:c.-3402_-3399dup
CYP7B1 transcript variant 2	NM_001324112.2:c.123-71065=	NM_001324112.2:c.123-71079_123-71065del	NM_001324112.2:c.123-71078_123-71065del	NM_001324112.2:c.123-71077_123-71065del	NM_001324112.2:c.123-71076_123-71065del	NM_001324112.2:c.123-71075_123-71065del	NM_001324112.2:c.123-71074_123-71065del	NM_001324112.2:c.123-71073_123-71065del	NM_001324112.2:c.123-71072_123-71065del	NM_001324112.2:c.123-71071_123-71065del	NM_001324112.2:c.123-71070_123-71065del	NM_001324112.2:c.123-71069_123-71065del	NM_001324112.2:c.123-71068_123-71065del	NM_001324112.2:c.123-71067_123-71065del	NM_001324112.2:c.123-71066_123-71065del	NM_001324112.2:c.123-71065del	NM_001324112.2:c.123-71065dup	NM_001324112.2:c.123-71066_123-71065dup	NM_001324112.2:c.123-71067_123-71065dup	NM_001324112.2:c.123-71068_123-71065dup
CYP7B1 transcript	NM_004820.3:c.123-71065=	NM_004820.3:c.123-71079_123-71065del	NM_004820.3:c.123-71078_123-71065del	NM_004820.3:c.123-71077_123-71065del	NM_004820.3:c.123-71076_123-71065del	NM_004820.3:c.123-71075_123-71065del	NM_004820.3:c.123-71074_123-71065del	NM_004820.3:c.123-71073_123-71065del	NM_004820.3:c.123-71072_123-71065del	NM_004820.3:c.123-71071_123-71065del	NM_004820.3:c.123-71070_123-71065del	NM_004820.3:c.123-71069_123-71065del	NM_004820.3:c.123-71068_123-71065del	NM_004820.3:c.123-71067_123-71065del	NM_004820.3:c.123-71066_123-71065del	NM_004820.3:c.123-71065del	NM_004820.3:c.123-71065dup	NM_004820.3:c.123-71066_123-71065dup	NM_004820.3:c.123-71067_123-71065dup	NM_004820.3:c.123-71068_123-71065dup
CYP7B1 transcript variant 1	NM_004820.5:c.123-71065=	NM_004820.5:c.123-71079_123-71065del	NM_004820.5:c.123-71078_123-71065del	NM_004820.5:c.123-71077_123-71065del	NM_004820.5:c.123-71076_123-71065del	NM_004820.5:c.123-71075_123-71065del	NM_004820.5:c.123-71074_123-71065del	NM_004820.5:c.123-71073_123-71065del	NM_004820.5:c.123-71072_123-71065del	NM_004820.5:c.123-71071_123-71065del	NM_004820.5:c.123-71070_123-71065del	NM_004820.5:c.123-71069_123-71065del	NM_004820.5:c.123-71068_123-71065del	NM_004820.5:c.123-71067_123-71065del	NM_004820.5:c.123-71066_123-71065del	NM_004820.5:c.123-71065del	NM_004820.5:c.123-71065dup	NM_004820.5:c.123-71066_123-71065dup	NM_004820.5:c.123-71067_123-71065dup	NM_004820.5:c.123-71068_123-71065dup

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#.

71 SubSNP, 41 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80511707	Aug 21, 2014 (142)
2	HUMANGENOME_JCVI	ss95494080	Mar 15, 2016 (147)
3	HUMANGENOME_JCVI	ss98027467	Mar 15, 2016 (147)
4	BCMHGSC_JDW	ss103769242	Mar 15, 2016 (147)
5	PJP	ss295384183	May 09, 2011 (137)
6	1000GENOMES	ss1367961231	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1706082899	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1706082964	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710384335	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710384336	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710384360	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710384362	Apr 01, 2015 (144)
13	SWEGEN	ss3003313528	Nov 08, 2017 (151)
14	MCHAISSO	ss3066205834	Nov 08, 2017 (151)
15	EVA_DECODE	ss3722175704	Jul 13, 2019 (153)
16	EVA_DECODE	ss3722175705	Jul 13, 2019 (153)
17	EVA_DECODE	ss3722175706	Jul 13, 2019 (153)
18	EVA_DECODE	ss3722175707	Jul 13, 2019 (153)
19	EVA_DECODE	ss3722175708	Jul 13, 2019 (153)
20	EVA_DECODE	ss3722175709	Jul 13, 2019 (153)
21	ACPOP	ss3735733316	Jul 13, 2019 (153)
22	ACPOP	ss3735733317	Jul 13, 2019 (153)
23	ACPOP	ss3735733318	Jul 13, 2019 (153)
24	PACBIO	ss3796300093	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3811258220	Jul 13, 2019 (153)
26	EVA	ss3831203825	Apr 26, 2020 (154)
27	GNOMAD	ss4185843188	Apr 26, 2021 (155)
28	GNOMAD	ss4185843189	Apr 26, 2021 (155)
29	GNOMAD	ss4185843190	Apr 26, 2021 (155)
30	GNOMAD	ss4185843191	Apr 26, 2021 (155)
31	GNOMAD	ss4185843193	Apr 26, 2021 (155)
32	GNOMAD	ss4185843194	Apr 26, 2021 (155)
33	GNOMAD	ss4185843195	Apr 26, 2021 (155)
34	GNOMAD	ss4185843196	Apr 26, 2021 (155)
35	GNOMAD	ss4185843197	Apr 26, 2021 (155)
36	GNOMAD	ss4185843198	Apr 26, 2021 (155)
37	GNOMAD	ss4185843199	Apr 26, 2021 (155)
38	GNOMAD	ss4185843200	Apr 26, 2021 (155)
39	GNOMAD	ss4185843201	Apr 26, 2021 (155)
40	GNOMAD	ss4185843202	Apr 26, 2021 (155)
41	GNOMAD	ss4185843203	Apr 26, 2021 (155)
42	GNOMAD	ss4185843204	Apr 26, 2021 (155)
43	GNOMAD	ss4185843205	Apr 26, 2021 (155)
44	GNOMAD	ss4185843206	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5189079265	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5189079266	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5189079267	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5189079268	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5189079269	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5189079270	Apr 26, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5277430381	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5277430382	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5277430383	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5473967655	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5473967656	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5473967657	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5473967658	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5473967659	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5473967660	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5731251161	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5731251162	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5731251163	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5731251164	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5731251165	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5731251166	Oct 16, 2022 (156)
66	EVA	ss5830646096	Oct 16, 2022 (156)
67	EVA	ss5830646097	Oct 16, 2022 (156)
68	EVA	ss5830646098	Oct 16, 2022 (156)
69	EVA	ss5830646099	Oct 16, 2022 (156)
70	EVA	ss5830646100	Oct 16, 2022 (156)
71	EVA	ss5889298726	Oct 16, 2022 (156)
72	1000Genomes	NC_000008.10 - 65608161	Oct 12, 2018 (152)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 23539344 (NC_000008.10:65608160:TTTTTTTTT: 389/3854) Row 23539345 (NC_000008.10:65608164:T: 1106/3854)	-	Oct 12, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 23539344 (NC_000008.10:65608160:TTTTTTTTT: 389/3854) Row 23539345 (NC_000008.10:65608164:T: 1106/3854)	-	Oct 12, 2018 (152)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298456954 (NC_000008.11:64695603::T 489/93494) Row 298456955 (NC_000008.11:64695603::TT 1914/93458) Row 298456956 (NC_000008.11:64695603::TTT 33/93508)...	-	Apr 26, 2021 (155)
94	Northern Sweden Submission ignored due to conflicting rows: Row 9018181 (NC_000008.10:65608160:TTTTTT: 2/590) Row 9018182 (NC_000008.10:65608160:TTTTT: 8/590) Row 9018183 (NC_000008.10:65608160:TT: 7/590)	-	Jul 13, 2019 (153)
95	Northern Sweden Submission ignored due to conflicting rows: Row 9018181 (NC_000008.10:65608160:TTTTTT: 2/590) Row 9018182 (NC_000008.10:65608160:TTTTT: 8/590) Row 9018183 (NC_000008.10:65608160:TT: 7/590)	-	Jul 13, 2019 (153)
96	Northern Sweden Submission ignored due to conflicting rows: Row 9018181 (NC_000008.10:65608160:TTTTTT: 2/590) Row 9018182 (NC_000008.10:65608160:TTTTT: 8/590) Row 9018183 (NC_000008.10:65608160:TT: 7/590)	-	Jul 13, 2019 (153)
97	8.3KJPN Submission ignored due to conflicting rows: Row 47048572 (NC_000008.10:65608160:TT: 1587/16086) Row 47048573 (NC_000008.10:65608160:T: 4524/16086) Row 47048574 (NC_000008.10:65608160::TT 2181/16086)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 47048572 (NC_000008.10:65608160:TT: 1587/16086) Row 47048573 (NC_000008.10:65608160:T: 4524/16086) Row 47048574 (NC_000008.10:65608160::TT 2181/16086)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 47048572 (NC_000008.10:65608160:TT: 1587/16086) Row 47048573 (NC_000008.10:65608160:T: 4524/16086) Row 47048574 (NC_000008.10:65608160::TT 2181/16086)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 47048572 (NC_000008.10:65608160:TT: 1587/16086) Row 47048573 (NC_000008.10:65608160:T: 4524/16086) Row 47048574 (NC_000008.10:65608160::TT 2181/16086)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 47048572 (NC_000008.10:65608160:TT: 1587/16086) Row 47048573 (NC_000008.10:65608160:T: 4524/16086) Row 47048574 (NC_000008.10:65608160::TT 2181/16086)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 47048572 (NC_000008.10:65608160:TT: 1587/16086) Row 47048573 (NC_000008.10:65608160:T: 4524/16086) Row 47048574 (NC_000008.10:65608160::TT 2181/16086)...	-	Apr 26, 2021 (155)
103	14KJPN Submission ignored due to conflicting rows: Row 65088265 (NC_000008.11:64695603:TTTTTTTT: 248/28234) Row 65088266 (NC_000008.11:64695603:TT: 3277/28234) Row 65088267 (NC_000008.11:64695603:T: 9592/28234)...	-	Oct 16, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 65088265 (NC_000008.11:64695603:TTTTTTTT: 248/28234) Row 65088266 (NC_000008.11:64695603:TT: 3277/28234) Row 65088267 (NC_000008.11:64695603:T: 9592/28234)...	-	Oct 16, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 65088265 (NC_000008.11:64695603:TTTTTTTT: 248/28234) Row 65088266 (NC_000008.11:64695603:TT: 3277/28234) Row 65088267 (NC_000008.11:64695603:T: 9592/28234)...	-	Oct 16, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 65088265 (NC_000008.11:64695603:TTTTTTTT: 248/28234) Row 65088266 (NC_000008.11:64695603:TT: 3277/28234) Row 65088267 (NC_000008.11:64695603:T: 9592/28234)...	-	Oct 16, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 65088265 (NC_000008.11:64695603:TTTTTTTT: 248/28234) Row 65088266 (NC_000008.11:64695603:TT: 3277/28234) Row 65088267 (NC_000008.11:64695603:T: 9592/28234)...	-	Oct 16, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 65088265 (NC_000008.11:64695603:TTTTTTTT: 248/28234) Row 65088266 (NC_000008.11:64695603:TT: 3277/28234) Row 65088267 (NC_000008.11:64695603:T: 9592/28234)...	-	Oct 16, 2022 (156)
109	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23539343 (NC_000008.10:65608166:TTT: 2140/3708) Row 23539344 (NC_000008.10:65608160:TTTTTTTTT: 324/3708) Row 23539345 (NC_000008.10:65608164:TTTTT: 1072/3708)	-	Apr 26, 2020 (154)
110	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23539344 (NC_000008.10:65608160:TTTTTTTTT: 324/3708) Row 23539345 (NC_000008.10:65608164:T: 1072/3708)	-	Oct 12, 2018 (152)
111	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23539344 (NC_000008.10:65608160:TTTTTTTTT: 324/3708) Row 23539345 (NC_000008.10:65608164:T: 1072/3708)	-	Oct 12, 2018 (152)
112	ALFA	NC_000008.11 - 64695604	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)
rs67736275	Oct 26, 2010 (133)
rs67736276	Feb 27, 2009 (130)
rs67736277	Feb 27, 2009 (130)
rs68098764	Jul 30, 2012 (137)
rs68098765	Feb 27, 2009 (130)
rs140874617	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4185843206	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4185843205	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3066205834, ss4185843204, ss5889298726	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4185843203	NC_000008.11:64695603:TTTTTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4185843202	NC_000008.11:64695603:TTTTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4185843201	NC_000008.11:64695603:TTTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss80511707	NC_000008.9:65770731:TTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
42325231, ss1367961231, ss1706082899, ss1706082964, ss3003313528, ss3831203825, ss5189079268, ss5830646096	NC_000008.10:65608160:TTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3722175704, ss3811258220, ss4185843200, ss5277430383, ss5473967655, ss5731251165	NC_000008.11:64695603:TTTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5189079269	NC_000008.10:65608160:TTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4185843199, ss5731251161	NC_000008.11:64695603:TTTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4185843198	NC_000008.11:64695603:TTTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3735733316, ss5830646100	NC_000008.10:65608160:TTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4185843197	NC_000008.11:64695603:TTTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3735733317, ss5830646099	NC_000008.10:65608160:TTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1710384336, ss1710384362	NC_000008.10:65608164:TTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843196, ss5277430382, ss5473967659	NC_000008.11:64695603:TTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3722175705	NC_000008.11:64695607:TTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss98027467	NT_008183.19:17472561:TTTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843195, ss5277430381, ss5473967660	NC_000008.11:64695603:TTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722175706	NC_000008.11:64695608:TTTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5189079270, ss5830646098	NC_000008.10:65608160:TTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710384335, ss1710384360	NC_000008.10:65608166:TTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843194, ss5473967656	NC_000008.11:64695603:TTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722175707	NC_000008.11:64695609:TTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss98027467	NT_008183.19:17472561:TTTTT:TT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95494080	NT_008183.19:17472584:TTT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3735733318, ss5189079265, ss5830646097	NC_000008.10:65608160:TT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843193, ss5473967657, ss5731251162	NC_000008.11:64695603:TT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722175708	NC_000008.11:64695610:TT:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295384183	NC_000008.9:65770714:T:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3796300093, ss5189079266	NC_000008.10:65608160:T:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000008.10:65608164:T:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5473967658, ss5731251163	NC_000008.11:64695603:T:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722175709	NC_000008.11:64695611:T:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103769242	NT_008183.19:17472564:T:	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843188, ss5731251166	NC_000008.11:64695603::T	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5189079267	NC_000008.10:65608160::TT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843189, ss5731251164	NC_000008.11:64695603::TT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843190	NC_000008.11:64695603::TTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185843191	NC_000008.11:64695603::TTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10114193050	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:64695603:TTTTTTTTTTTT… NC_000008.11:64695603:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs35575527

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

rs35575527