Name: rs67496918
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.

rs67496918

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:45166782-45166809 (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)₁₁ / del(T)₁₀ / del(T)₉ / de…
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)₁₀ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₁=0.00000 (0/11000, ALFA)
del(T)₁₀=0.00000 (0/11000, ALFA)
del(T)₉=0.00000 (0/11000, ALFA) (+ 13 more)
del(T)₈=0.00000 (0/11000, ALFA)
del(T)₇=0.00000 (0/11000, ALFA)
del(T)₆=0.00000 (0/11000, ALFA)
del(T)₅=0.00000 (0/11000, ALFA)
del(T)₄=0.00000 (0/11000, ALFA)
delTTT=0.00000 (0/11000, ALFA)
delTT=0.00000 (0/11000, ALFA)
delT=0.00000 (0/11000, ALFA)
dupT=0.00000 (0/11000, ALFA)
dupTT=0.00000 (0/11000, ALFA)
dupTTT=0.00000 (0/11000, ALFA)
dup(T)₄=0.00000 (0/11000, ALFA)
dup(T)₅=0.00000 (0/11000, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ANKRD30BP3 : 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	HWEP
Total	Global	11000	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7386	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2352	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	86	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2266	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	84	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	66	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	138	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	538	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	80	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	422	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11000	(T)₂₈=1.00000	del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000
Allele Frequency Aggregator	European	Sub	7386	(T)₂₈=1.0000	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=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	2352	(T)₂₈=1.0000	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=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	538	(T)₂₈=1.000	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, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	422	(T)₂₈=1.000	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, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(T)₂₈=1.000	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, dup(T)₅=0.000
Allele Frequency Aggregator	Asian	Sub	84	(T)₂₈=1.00	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, dup(T)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	80	(T)₂₈=1.00	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, dup(T)₅=0.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.45166799_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166800_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166801_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166802_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166803_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166804_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166805_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166806_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166807_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166808_45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166809del
GRCh38.p14 chr 10	NC_000010.11:g.45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166808_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166807_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166806_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166805_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166804_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166803_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166802_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166801_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166800_45166809dup
GRCh38.p14 chr 10	NC_000010.11:g.45166799_45166809dup
GRCh37.p13 chr 10	NC_000010.10:g.45662247_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662248_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662249_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662250_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662251_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662252_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662253_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662254_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662255_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662256_45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662257del
GRCh37.p13 chr 10	NC_000010.10:g.45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662256_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662255_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662254_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662253_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662252_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662251_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662250_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662249_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662248_45662257dup
GRCh37.p13 chr 10	NC_000010.10:g.45662247_45662257dup

Gene: ANKRD30BP3, ankyrin repeat domain 30B pseudogene 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ANKRD30BP3 transcript	NR_033891.1:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₈=	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)₁₀	dup(T)₁₁
GRCh38.p14 chr 10	NC_000010.11:g.45166782_45166809=	NC_000010.11:g.45166799_45166809del	NC_000010.11:g.45166800_45166809del	NC_000010.11:g.45166801_45166809del	NC_000010.11:g.45166802_45166809del	NC_000010.11:g.45166803_45166809del	NC_000010.11:g.45166804_45166809del	NC_000010.11:g.45166805_45166809del	NC_000010.11:g.45166806_45166809del	NC_000010.11:g.45166807_45166809del	NC_000010.11:g.45166808_45166809del	NC_000010.11:g.45166809del	NC_000010.11:g.45166809dup	NC_000010.11:g.45166808_45166809dup	NC_000010.11:g.45166807_45166809dup	NC_000010.11:g.45166806_45166809dup	NC_000010.11:g.45166805_45166809dup	NC_000010.11:g.45166804_45166809dup	NC_000010.11:g.45166803_45166809dup	NC_000010.11:g.45166802_45166809dup	NC_000010.11:g.45166801_45166809dup	NC_000010.11:g.45166800_45166809dup	NC_000010.11:g.45166799_45166809dup
GRCh37.p13 chr 10	NC_000010.10:g.45662230_45662257=	NC_000010.10:g.45662247_45662257del	NC_000010.10:g.45662248_45662257del	NC_000010.10:g.45662249_45662257del	NC_000010.10:g.45662250_45662257del	NC_000010.10:g.45662251_45662257del	NC_000010.10:g.45662252_45662257del	NC_000010.10:g.45662253_45662257del	NC_000010.10:g.45662254_45662257del	NC_000010.10:g.45662255_45662257del	NC_000010.10:g.45662256_45662257del	NC_000010.10:g.45662257del	NC_000010.10:g.45662257dup	NC_000010.10:g.45662256_45662257dup	NC_000010.10:g.45662255_45662257dup	NC_000010.10:g.45662254_45662257dup	NC_000010.10:g.45662253_45662257dup	NC_000010.10:g.45662252_45662257dup	NC_000010.10:g.45662251_45662257dup	NC_000010.10:g.45662250_45662257dup	NC_000010.10:g.45662249_45662257dup	NC_000010.10:g.45662248_45662257dup	NC_000010.10:g.45662247_45662257dup

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#.

37 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95539864	Feb 05, 2009 (130)
2	HUMANGENOME_JCVI	ss97603373	Feb 05, 2009 (130)
3	PJP	ss294654146	May 09, 2011 (137)
4	KOGIC	ss3967783324	Apr 26, 2020 (154)
5	KOGIC	ss3967783325	Apr 26, 2020 (154)
6	KOGIC	ss3967783326	Apr 26, 2020 (154)
7	GNOMAD	ss4217468492	Apr 26, 2021 (155)
8	GNOMAD	ss4217468493	Apr 26, 2021 (155)
9	GNOMAD	ss4217468494	Apr 26, 2021 (155)
10	GNOMAD	ss4217468495	Apr 26, 2021 (155)
11	GNOMAD	ss4217468496	Apr 26, 2021 (155)
12	GNOMAD	ss4217468497	Apr 26, 2021 (155)
13	GNOMAD	ss4217468498	Apr 26, 2021 (155)
14	GNOMAD	ss4217468499	Apr 26, 2021 (155)
15	GNOMAD	ss4217468500	Apr 26, 2021 (155)
16	GNOMAD	ss4217468501	Apr 26, 2021 (155)
17	GNOMAD	ss4217468502	Apr 26, 2021 (155)
18	GNOMAD	ss4217468504	Apr 26, 2021 (155)
19	GNOMAD	ss4217468505	Apr 26, 2021 (155)
20	GNOMAD	ss4217468506	Apr 26, 2021 (155)
21	GNOMAD	ss4217468507	Apr 26, 2021 (155)
22	GNOMAD	ss4217468508	Apr 26, 2021 (155)
23	GNOMAD	ss4217468509	Apr 26, 2021 (155)
24	GNOMAD	ss4217468510	Apr 26, 2021 (155)
25	GNOMAD	ss4217468511	Apr 26, 2021 (155)
26	GNOMAD	ss4217468512	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5197394814	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5197394815	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5197394816	Apr 26, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5283851575	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5283851576	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5283851577	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5283851578	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5743147686	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5743147687	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5743147688	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5743147689	Oct 16, 2022 (156)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 350737388 (NC_000010.11:45166781::T 897/102218) Row 350737389 (NC_000010.11:45166781::TT 37/102264) Row 350737390 (NC_000010.11:45166781::TTT 92/102268)...	-	Apr 26, 2021 (155)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 24161325 (NC_000010.11:45166783:TT: 74/1674) Row 24161326 (NC_000010.11:45166782:TTT: 11/1674) Row 24161327 (NC_000010.11:45166784:T: 28/1674)	-	Apr 26, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 24161325 (NC_000010.11:45166783:TT: 74/1674) Row 24161326 (NC_000010.11:45166782:TTT: 11/1674) Row 24161327 (NC_000010.11:45166784:T: 28/1674)	-	Apr 26, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 24161325 (NC_000010.11:45166783:TT: 74/1674) Row 24161326 (NC_000010.11:45166782:TTT: 11/1674) Row 24161327 (NC_000010.11:45166784:T: 28/1674)	-	Apr 26, 2020 (154)
62	8.3KJPN Submission ignored due to conflicting rows: Row 55364121 (NC_000010.10:45662229:TT: 349/15690) Row 55364122 (NC_000010.10:45662229:TTT: 131/15690) Row 55364123 (NC_000010.10:45662229:T: 49/15690)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 55364121 (NC_000010.10:45662229:TT: 349/15690) Row 55364122 (NC_000010.10:45662229:TTT: 131/15690) Row 55364123 (NC_000010.10:45662229:T: 49/15690)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 55364121 (NC_000010.10:45662229:TT: 349/15690) Row 55364122 (NC_000010.10:45662229:TTT: 131/15690) Row 55364123 (NC_000010.10:45662229:T: 49/15690)	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 76984790 (NC_000010.11:45166781:TTT: 331/25454) Row 76984791 (NC_000010.11:45166781:TT: 881/25454) Row 76984792 (NC_000010.11:45166781:T: 107/25454)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 76984790 (NC_000010.11:45166781:TTT: 331/25454) Row 76984791 (NC_000010.11:45166781:TT: 881/25454) Row 76984792 (NC_000010.11:45166781:T: 107/25454)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 76984790 (NC_000010.11:45166781:TTT: 331/25454) Row 76984791 (NC_000010.11:45166781:TT: 881/25454) Row 76984792 (NC_000010.11:45166781:T: 107/25454)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 76984790 (NC_000010.11:45166781:TTT: 331/25454) Row 76984791 (NC_000010.11:45166781:TT: 881/25454) Row 76984792 (NC_000010.11:45166781:T: 107/25454)...	-	Oct 16, 2022 (156)
69	ALFA	NC_000010.11 - 45166782	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)
rs67496919	Feb 27, 2009 (130)
rs148973587	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4217468512	NC_000010.11:45166781:TTTTTTTTTTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4217468511, ss5283851578	NC_000010.11:45166781:TTTTTTTTTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4217468510	NC_000010.11:45166781:TTTTTTTTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4217468509	NC_000010.11:45166781:TTTTTTTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4217468508	NC_000010.11:45166781:TTTTTTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468507	NC_000010.11:45166781:TTTTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468506	NC_000010.11:45166781:TTTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5197394815	NC_000010.10:45662229:TTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468505, ss5743147686	NC_000010.11:45166781:TTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3967783325	NC_000010.11:45166782:TTT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5197394814	NC_000010.10:45662229:TT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468504, ss5283851577, ss5743147687	NC_000010.11:45166781:TT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3967783324	NC_000010.11:45166783:TT:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5197394816	NC_000010.10:45662229:T:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5283851576, ss5743147688	NC_000010.11:45166781:T:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3967783326	NC_000010.11:45166784:T:	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294654146	NC_000010.9:44982236::T	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468492, ss5283851575	NC_000010.11:45166781::T	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss97603373	NT_033985.7:3307321::T	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95539864	NT_033985.7:3307322::T	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468493	NC_000010.11:45166781::TT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468494	NC_000010.11:45166781::TTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468495	NC_000010.11:45166781::TTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468496, ss5743147689	NC_000010.11:45166781::TTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4109178355	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468497	NC_000010.11:45166781::TTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468498	NC_000010.11:45166781::TTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468499	NC_000010.11:45166781::TTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468500	NC_000010.11:45166781::TTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468501	NC_000010.11:45166781::TTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4217468502	NC_000010.11:45166781::TTTTTTTTTTT	NC_000010.11:45166781:TTTTTTTTTTTT… NC_000010.11:45166781:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs67496918

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

rs67496918