Name: rs67032351
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.

rs67032351

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:40848941-40848977 (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(GA)₁₀ / del(GA)₉ / del(GA)₈ / …
del(GA)₁₀ / del(GA)₉ / del(GA)₈ / del(GA)₇ / del(GA)₆ / del(GA)₅ / del(GA)₄ / del(GA)₃ / delGAGA / delGA / dupGA / dupGAGA / dup(GA)₃ / dup(GA)₄ / dup(GA)₅ / dup(GA)₆ / dup(GA)₇ / dup(GA)₈ / dup(GA)₉
Variation Type: Indel Insertion and Deletion
Frequency: (AG)₁₈A=0.3263 (1634/5008, 1000G)
del(GA)₁₀=0.000 (0/382, ALFA)
del(GA)₉=0.000 (0/382, ALFA) (+ 13 more)
del(GA)₈=0.000 (0/382, ALFA)
del(GA)₇=0.000 (0/382, ALFA)
del(GA)₆=0.000 (0/382, ALFA)
del(GA)₅=0.000 (0/382, ALFA)
del(GA)₄=0.000 (0/382, ALFA)
del(GA)₃=0.000 (0/382, ALFA)
delGAGA=0.000 (0/382, ALFA)
delGA=0.000 (0/382, ALFA)
dupGA=0.000 (0/382, ALFA)
dupGAGA=0.000 (0/382, ALFA)
dup(GA)₃=0.000 (0/382, ALFA)
dup(GA)₄=0.000 (0/382, ALFA)
dup(GA)₅=0.000 (0/382, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP2A6 : 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	382	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.000	AGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000	1.0	0.0	0.0	N/A
European	Sub	86	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	0.0	0.0	N/A
African	Sub	272	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.000	AGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	14	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	0.0	0.0	N/A
African American	Sub	258	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.000	AGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.0	AGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.0	AGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	AGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	0	0	0	N/A
Latin American 1	Sub	0	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	AGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	0	0	0	N/A
Latin American 2	Sub	8	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.0	AGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	AGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	0	0	0	N/A
Other	Sub	14	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(AG)₁₈A=0.3263	delGAGA=0.6737
1000Genomes	African	Sub	1322	(AG)₁₈A=0.4244	delGAGA=0.5756
1000Genomes	East Asian	Sub	1008	(AG)₁₈A=0.3859	delGAGA=0.6141
1000Genomes	Europe	Sub	1006	(AG)₁₈A=0.2306	delGAGA=0.7694
1000Genomes	South Asian	Sub	978	(AG)₁₈A=0.316	delGAGA=0.684
1000Genomes	American	Sub	694	(AG)₁₈A=0.206	delGAGA=0.794
Allele Frequency Aggregator	Total	Global	382	(AG)₁₈A=1.000	del(GA)₁₀=0.000, del(GA)₉=0.000, del(GA)₈=0.000, del(GA)₇=0.000, del(GA)₆=0.000, del(GA)₅=0.000, del(GA)₄=0.000, del(GA)₃=0.000, delGAGA=0.000, delGA=0.000, dupGA=0.000, dupGAGA=0.000, dup(GA)₃=0.000, dup(GA)₄=0.000, dup(GA)₅=0.000
Allele Frequency Aggregator	African	Sub	272	(AG)₁₈A=1.000	del(GA)₁₀=0.000, del(GA)₉=0.000, del(GA)₈=0.000, del(GA)₇=0.000, del(GA)₆=0.000, del(GA)₅=0.000, del(GA)₄=0.000, del(GA)₃=0.000, delGAGA=0.000, delGA=0.000, dupGA=0.000, dupGAGA=0.000, dup(GA)₃=0.000, dup(GA)₄=0.000, dup(GA)₅=0.000
Allele Frequency Aggregator	European	Sub	86	(AG)₁₈A=1.00	del(GA)₁₀=0.00, del(GA)₉=0.00, del(GA)₈=0.00, del(GA)₇=0.00, del(GA)₆=0.00, del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.00, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.00, dup(GA)₃=0.00, dup(GA)₄=0.00, dup(GA)₅=0.00
Allele Frequency Aggregator	Other	Sub	14	(AG)₁₈A=1.00	del(GA)₁₀=0.00, del(GA)₉=0.00, del(GA)₈=0.00, del(GA)₇=0.00, del(GA)₆=0.00, del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.00, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.00, dup(GA)₃=0.00, dup(GA)₄=0.00, dup(GA)₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	8	(AG)₁₈A=1.0	del(GA)₁₀=0.0, del(GA)₉=0.0, del(GA)₈=0.0, del(GA)₇=0.0, del(GA)₆=0.0, del(GA)₅=0.0, del(GA)₄=0.0, del(GA)₃=0.0, delGAGA=0.0, delGA=0.0, dupGA=0.0, dupGAGA=0.0, dup(GA)₃=0.0, dup(GA)₄=0.0, dup(GA)₅=0.0
Allele Frequency Aggregator	Asian	Sub	2	(AG)₁₈A=1.0	del(GA)₁₀=0.0, del(GA)₉=0.0, del(GA)₈=0.0, del(GA)₇=0.0, del(GA)₆=0.0, del(GA)₅=0.0, del(GA)₄=0.0, del(GA)₃=0.0, delGAGA=0.0, delGA=0.0, dupGA=0.0, dupGAGA=0.0, dup(GA)₃=0.0, dup(GA)₄=0.0, dup(GA)₅=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(AG)₁₈A=0	del(GA)₁₀=0, del(GA)₉=0, del(GA)₈=0, del(GA)₇=0, del(GA)₆=0, del(GA)₅=0, del(GA)₄=0, del(GA)₃=0, delGAGA=0, delGA=0, dupGA=0, dupGAGA=0, dup(GA)₃=0, dup(GA)₄=0, dup(GA)₅=0
Allele Frequency Aggregator	South Asian	Sub	0	(AG)₁₈A=0	del(GA)₁₀=0, del(GA)₉=0, del(GA)₈=0, del(GA)₇=0, del(GA)₆=0, del(GA)₅=0, del(GA)₄=0, del(GA)₃=0, delGAGA=0, delGA=0, dupGA=0, dupGAGA=0, dup(GA)₃=0, dup(GA)₄=0, dup(GA)₅=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 19	NC_000019.10:g.40848942GA[8]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[9]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[10]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[11]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[12]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[13]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[14]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[15]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[16]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[17]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[19]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[20]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[21]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[22]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[23]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[24]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[25]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[26]
GRCh38.p14 chr 19	NC_000019.10:g.40848942GA[27]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[8]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[9]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[10]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[11]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[12]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[13]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[14]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[15]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[16]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[17]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[19]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[20]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[21]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[22]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[23]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[24]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[25]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[26]
GRCh37.p13 chr 19	NC_000019.9:g.41354847GA[27]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[8]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[9]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[10]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[11]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[12]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[13]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[14]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[15]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[16]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[17]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[19]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[20]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[21]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[22]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[23]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[24]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[25]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[26]
CYP2A6 RefSeqGene	NG_008377.1:g.6472CT[27]

Gene: CYP2A6, cytochrome P450 family 2 subfamily A member 6 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CYP2A6 transcript	NM_000762.6:c.344-213CT[8]	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	(AG)₁₈A=	del(GA)₁₀	del(GA)₉	del(GA)₈	del(GA)₇	del(GA)₆	del(GA)₅	del(GA)₄	del(GA)₃	delGAGA	delGA	dupGA	dupGAGA	dup(GA)₃	dup(GA)₄	dup(GA)₅	dup(GA)₆	dup(GA)₇	dup(GA)₈	dup(GA)₉
GRCh38.p14 chr 19	NC_000019.10:g.40848941_40848977=	NC_000019.10:g.40848942GA[8]	NC_000019.10:g.40848942GA[9]	NC_000019.10:g.40848942GA[10]	NC_000019.10:g.40848942GA[11]	NC_000019.10:g.40848942GA[12]	NC_000019.10:g.40848942GA[13]	NC_000019.10:g.40848942GA[14]	NC_000019.10:g.40848942GA[15]	NC_000019.10:g.40848942GA[16]	NC_000019.10:g.40848942GA[17]	NC_000019.10:g.40848942GA[19]	NC_000019.10:g.40848942GA[20]	NC_000019.10:g.40848942GA[21]	NC_000019.10:g.40848942GA[22]	NC_000019.10:g.40848942GA[23]	NC_000019.10:g.40848942GA[24]	NC_000019.10:g.40848942GA[25]	NC_000019.10:g.40848942GA[26]	NC_000019.10:g.40848942GA[27]
GRCh37.p13 chr 19	NC_000019.9:g.41354846_41354882=	NC_000019.9:g.41354847GA[8]	NC_000019.9:g.41354847GA[9]	NC_000019.9:g.41354847GA[10]	NC_000019.9:g.41354847GA[11]	NC_000019.9:g.41354847GA[12]	NC_000019.9:g.41354847GA[13]	NC_000019.9:g.41354847GA[14]	NC_000019.9:g.41354847GA[15]	NC_000019.9:g.41354847GA[16]	NC_000019.9:g.41354847GA[17]	NC_000019.9:g.41354847GA[19]	NC_000019.9:g.41354847GA[20]	NC_000019.9:g.41354847GA[21]	NC_000019.9:g.41354847GA[22]	NC_000019.9:g.41354847GA[23]	NC_000019.9:g.41354847GA[24]	NC_000019.9:g.41354847GA[25]	NC_000019.9:g.41354847GA[26]	NC_000019.9:g.41354847GA[27]
CYP2A6 RefSeqGene	NG_008377.1:g.6471_6507=	NG_008377.1:g.6472CT[8]	NG_008377.1:g.6472CT[9]	NG_008377.1:g.6472CT[10]	NG_008377.1:g.6472CT[11]	NG_008377.1:g.6472CT[12]	NG_008377.1:g.6472CT[13]	NG_008377.1:g.6472CT[14]	NG_008377.1:g.6472CT[15]	NG_008377.1:g.6472CT[16]	NG_008377.1:g.6472CT[17]	NG_008377.1:g.6472CT[19]	NG_008377.1:g.6472CT[20]	NG_008377.1:g.6472CT[21]	NG_008377.1:g.6472CT[22]	NG_008377.1:g.6472CT[23]	NG_008377.1:g.6472CT[24]	NG_008377.1:g.6472CT[25]	NG_008377.1:g.6472CT[26]	NG_008377.1:g.6472CT[27]
CYP2A6 transcript	NM_000762.5:c.344-178=	NM_000762.5:c.344-213CT[8]	NM_000762.5:c.344-213CT[9]	NM_000762.5:c.344-213CT[10]	NM_000762.5:c.344-213CT[11]	NM_000762.5:c.344-213CT[12]	NM_000762.5:c.344-213CT[13]	NM_000762.5:c.344-213CT[14]	NM_000762.5:c.344-213CT[15]	NM_000762.5:c.344-213CT[16]	NM_000762.5:c.344-213CT[17]	NM_000762.5:c.344-213CT[19]	NM_000762.5:c.344-213CT[20]	NM_000762.5:c.344-213CT[21]	NM_000762.5:c.344-213CT[22]	NM_000762.5:c.344-213CT[23]	NM_000762.5:c.344-213CT[24]	NM_000762.5:c.344-213CT[25]	NM_000762.5:c.344-213CT[26]	NM_000762.5:c.344-213CT[27]
CYP2A6 transcript	NM_000762.6:c.344-178=	NM_000762.6:c.344-213CT[8]	NM_000762.6:c.344-213CT[9]	NM_000762.6:c.344-213CT[10]	NM_000762.6:c.344-213CT[11]	NM_000762.6:c.344-213CT[12]	NM_000762.6:c.344-213CT[13]	NM_000762.6:c.344-213CT[14]	NM_000762.6:c.344-213CT[15]	NM_000762.6:c.344-213CT[16]	NM_000762.6:c.344-213CT[17]	NM_000762.6:c.344-213CT[19]	NM_000762.6:c.344-213CT[20]	NM_000762.6:c.344-213CT[21]	NM_000762.6:c.344-213CT[22]	NM_000762.6:c.344-213CT[23]	NM_000762.6:c.344-213CT[24]	NM_000762.6:c.344-213CT[25]	NM_000762.6:c.344-213CT[26]	NM_000762.6:c.344-213CT[27]
CYP2A6 transcript variant X1	XM_005258568.1:c.191-178=	XM_005258568.1:c.191-213CT[8]	XM_005258568.1:c.191-213CT[9]	XM_005258568.1:c.191-213CT[10]	XM_005258568.1:c.191-213CT[11]	XM_005258568.1:c.191-213CT[12]	XM_005258568.1:c.191-213CT[13]	XM_005258568.1:c.191-213CT[14]	XM_005258568.1:c.191-213CT[15]	XM_005258568.1:c.191-213CT[16]	XM_005258568.1:c.191-213CT[17]	XM_005258568.1:c.191-213CT[19]	XM_005258568.1:c.191-213CT[20]	XM_005258568.1:c.191-213CT[21]	XM_005258568.1:c.191-213CT[22]	XM_005258568.1:c.191-213CT[23]	XM_005258568.1:c.191-213CT[24]	XM_005258568.1:c.191-213CT[25]	XM_005258568.1:c.191-213CT[26]	XM_005258568.1:c.191-213CT[27]

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

77 SubSNP, 43 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95728915	Feb 13, 2009 (130)
2	RTYNDALE	ss104807062	Feb 13, 2009 (130)
3	1000GENOMES	ss328033430	May 09, 2011 (135)
4	1000GENOMES	ss328277040	May 09, 2011 (135)
5	LUNTER	ss552626535	Apr 25, 2013 (138)
6	1000GENOMES	ss1378156616	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1709207152	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1709207445	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710792561	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710792563	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710792566	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710792569	Apr 01, 2015 (144)
13	AFFY	ss2985772741	Nov 08, 2017 (151)
14	SWEGEN	ss3017486454	Nov 08, 2017 (151)
15	MCHAISSO	ss3064764638	Nov 08, 2017 (151)
16	URBANLAB	ss3650919794	Oct 12, 2018 (152)
17	EVA_DECODE	ss3702784513	Jul 13, 2019 (153)
18	EVA_DECODE	ss3702784514	Jul 13, 2019 (153)
19	EVA_DECODE	ss3702784515	Jul 13, 2019 (153)
20	EVA_DECODE	ss3702784516	Jul 13, 2019 (153)
21	EVA_DECODE	ss3702784517	Jul 13, 2019 (153)
22	EVA_DECODE	ss3702784518	Jul 13, 2019 (153)
23	ACPOP	ss3743046270	Jul 13, 2019 (153)
24	ACPOP	ss3743046271	Jul 13, 2019 (153)
25	ACPOP	ss3743046272	Jul 13, 2019 (153)
26	ACPOP	ss3743046273	Jul 13, 2019 (153)
27	ACPOP	ss3743046274	Jul 13, 2019 (153)
28	PACBIO	ss3788533421	Jul 13, 2019 (153)
29	PACBIO	ss3793443415	Jul 13, 2019 (153)
30	PACBIO	ss3793443416	Jul 13, 2019 (153)
31	PACBIO	ss3798330236	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3821322030	Jul 13, 2019 (153)
33	GNOMAD	ss4331367360	Apr 26, 2021 (155)
34	GNOMAD	ss4331367361	Apr 26, 2021 (155)
35	GNOMAD	ss4331367362	Apr 26, 2021 (155)
36	GNOMAD	ss4331367363	Apr 26, 2021 (155)
37	GNOMAD	ss4331367364	Apr 26, 2021 (155)
38	GNOMAD	ss4331367365	Apr 26, 2021 (155)
39	GNOMAD	ss4331367366	Apr 26, 2021 (155)
40	GNOMAD	ss4331367367	Apr 26, 2021 (155)
41	GNOMAD	ss4331367368	Apr 26, 2021 (155)
42	GNOMAD	ss4331367370	Apr 26, 2021 (155)
43	GNOMAD	ss4331367371	Apr 26, 2021 (155)
44	GNOMAD	ss4331367372	Apr 26, 2021 (155)
45	GNOMAD	ss4331367373	Apr 26, 2021 (155)
46	GNOMAD	ss4331367374	Apr 26, 2021 (155)
47	GNOMAD	ss4331367375	Apr 26, 2021 (155)
48	GNOMAD	ss4331367376	Apr 26, 2021 (155)
49	GNOMAD	ss4331367377	Apr 26, 2021 (155)
50	GNOMAD	ss4331367378	Apr 26, 2021 (155)
51	GNOMAD	ss4331367379	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5227798782	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5227798783	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5227798784	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5227798785	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5227798786	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5227798787	Apr 26, 2021 (155)
58	1000G_HIGH_COVERAGE	ss5307276226	Oct 16, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5307276227	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5307276228	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5499798133	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5499798134	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5499798135	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5499798136	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5499798137	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5786445009	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5786445010	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5786445011	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5786445012	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5786445013	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5786445014	Oct 16, 2022 (156)
72	EVA	ss5840561321	Oct 16, 2022 (156)
73	EVA	ss5840561322	Oct 16, 2022 (156)
74	EVA	ss5840561323	Oct 16, 2022 (156)
75	EVA	ss5840561324	Oct 16, 2022 (156)
76	EVA	ss5852293693	Oct 16, 2022 (156)
77	EVA	ss5981054184	Oct 16, 2022 (156)
78	1000Genomes	NC_000019.9 - 41354846	Oct 12, 2018 (152)
79	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42428497 (NC_000019.9:41354845:AGAGAGAGAG: 269/3854) Row 42428498 (NC_000019.9:41354849:AG: 1786/3854)	-	Oct 12, 2018 (152)
80	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42428497 (NC_000019.9:41354845:AGAGAGAGAG: 269/3854) Row 42428498 (NC_000019.9:41354849:AG: 1786/3854)	-	Oct 12, 2018 (152)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540285847 (NC_000019.10:40848940::AG 544/61720) Row 540285848 (NC_000019.10:40848940::AGAG 244/61720) Row 540285849 (NC_000019.10:40848940::AGAGAG 23/61720)...	-	Apr 26, 2021 (155)
100	Northern Sweden Submission ignored due to conflicting rows: Row 16331135 (NC_000019.9:41354845:AGAGAGAGAG: 38/574) Row 16331136 (NC_000019.9:41354845:AG: 159/574) Row 16331137 (NC_000019.9:41354845:AGAG: 137/574)...	-	Jul 13, 2019 (153)
101	Northern Sweden Submission ignored due to conflicting rows: Row 16331135 (NC_000019.9:41354845:AGAGAGAGAG: 38/574) Row 16331136 (NC_000019.9:41354845:AG: 159/574) Row 16331137 (NC_000019.9:41354845:AGAG: 137/574)...	-	Jul 13, 2019 (153)
102	Northern Sweden Submission ignored due to conflicting rows: Row 16331135 (NC_000019.9:41354845:AGAGAGAGAG: 38/574) Row 16331136 (NC_000019.9:41354845:AG: 159/574) Row 16331137 (NC_000019.9:41354845:AGAG: 137/574)...	-	Jul 13, 2019 (153)
103	Northern Sweden Submission ignored due to conflicting rows: Row 16331135 (NC_000019.9:41354845:AGAGAGAGAG: 38/574) Row 16331136 (NC_000019.9:41354845:AG: 159/574) Row 16331137 (NC_000019.9:41354845:AGAG: 137/574)...	-	Jul 13, 2019 (153)
104	Northern Sweden Submission ignored due to conflicting rows: Row 16331135 (NC_000019.9:41354845:AGAGAGAGAG: 38/574) Row 16331136 (NC_000019.9:41354845:AG: 159/574) Row 16331137 (NC_000019.9:41354845:AGAG: 137/574)...	-	Jul 13, 2019 (153)
105	8.3KJPN Submission ignored due to conflicting rows: Row 85768089 (NC_000019.9:41354845:AGAGAGAGAG: 2740/13484) Row 85768090 (NC_000019.9:41354845::AG 1108/13484) Row 85768091 (NC_000019.9:41354845::AGAG 353/13484)...	-	Apr 26, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 85768089 (NC_000019.9:41354845:AGAGAGAGAG: 2740/13484) Row 85768090 (NC_000019.9:41354845::AG 1108/13484) Row 85768091 (NC_000019.9:41354845::AGAG 353/13484)...	-	Apr 26, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 85768089 (NC_000019.9:41354845:AGAGAGAGAG: 2740/13484) Row 85768090 (NC_000019.9:41354845::AG 1108/13484) Row 85768091 (NC_000019.9:41354845::AGAG 353/13484)...	-	Apr 26, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 85768089 (NC_000019.9:41354845:AGAGAGAGAG: 2740/13484) Row 85768090 (NC_000019.9:41354845::AG 1108/13484) Row 85768091 (NC_000019.9:41354845::AGAG 353/13484)...	-	Apr 26, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 85768089 (NC_000019.9:41354845:AGAGAGAGAG: 2740/13484) Row 85768090 (NC_000019.9:41354845::AG 1108/13484) Row 85768091 (NC_000019.9:41354845::AGAG 353/13484)...	-	Apr 26, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 85768089 (NC_000019.9:41354845:AGAGAGAGAG: 2740/13484) Row 85768090 (NC_000019.9:41354845::AG 1108/13484) Row 85768091 (NC_000019.9:41354845::AGAG 353/13484)...	-	Apr 26, 2021 (155)
111	14KJPN Submission ignored due to conflicting rows: Row 120282113 (NC_000019.10:40848940:AGAGAG: 881/21110) Row 120282114 (NC_000019.10:40848940::AG 1522/21110) Row 120282115 (NC_000019.10:40848940:AGAGAGAGAG: 3577/21110)...	-	Oct 16, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 120282113 (NC_000019.10:40848940:AGAGAG: 881/21110) Row 120282114 (NC_000019.10:40848940::AG 1522/21110) Row 120282115 (NC_000019.10:40848940:AGAGAGAGAG: 3577/21110)...	-	Oct 16, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 120282113 (NC_000019.10:40848940:AGAGAG: 881/21110) Row 120282114 (NC_000019.10:40848940::AG 1522/21110) Row 120282115 (NC_000019.10:40848940:AGAGAGAGAG: 3577/21110)...	-	Oct 16, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 120282113 (NC_000019.10:40848940:AGAGAG: 881/21110) Row 120282114 (NC_000019.10:40848940::AG 1522/21110) Row 120282115 (NC_000019.10:40848940:AGAGAGAGAG: 3577/21110)...	-	Oct 16, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 120282113 (NC_000019.10:40848940:AGAGAG: 881/21110) Row 120282114 (NC_000019.10:40848940::AG 1522/21110) Row 120282115 (NC_000019.10:40848940:AGAGAGAGAG: 3577/21110)...	-	Oct 16, 2022 (156)
116	14KJPN Submission ignored due to conflicting rows: Row 120282113 (NC_000019.10:40848940:AGAGAG: 881/21110) Row 120282114 (NC_000019.10:40848940::AG 1522/21110) Row 120282115 (NC_000019.10:40848940:AGAGAGAGAG: 3577/21110)...	-	Oct 16, 2022 (156)
117	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42428496 (NC_000019.9:41354851:AGAG: 1500/3708) Row 42428497 (NC_000019.9:41354845:AGAGAGAGAG: 326/3708) Row 42428498 (NC_000019.9:41354849:AGAGAG: 1706/3708)	-	Apr 27, 2020 (154)
118	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42428497 (NC_000019.9:41354845:AGAGAGAGAG: 326/3708) Row 42428498 (NC_000019.9:41354849:AG: 1706/3708)	-	Oct 12, 2018 (152)
119	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42428497 (NC_000019.9:41354845:AGAGAGAGAG: 326/3708) Row 42428498 (NC_000019.9:41354849:AG: 1706/3708)	-	Oct 12, 2018 (152)
120	ALFA	NC_000019.10 - 40848941	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)
rs67032352	Feb 26, 2009 (130)
rs145221661	Sep 17, 2011 (135)
rs148825645	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4331367379	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss4331367378	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA	(self)
ss4331367377	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367376	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367375	NC_000019.10:40848940:AGAGAGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss1709207152, ss1709207445, ss3017486454, ss3743046270, ss5227798782, ss5840561324	NC_000019.9:41354845:AGAGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3702784518, ss4331367374, ss5307276226, ss5499798133, ss5786445011	NC_000019.10:40848940:AGAGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3743046274	NC_000019.9:41354845:AGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367373, ss5307276227, ss5499798137	NC_000019.10:40848940:AGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3702784517	NC_000019.10:40848942:AGAGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss328277040	NC_000019.8:46046685:AGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss2985772741, ss3743046273, ss5227798785, ss5840561321	NC_000019.9:41354845:AGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss1710792563, ss1710792569	NC_000019.9:41354849:AGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3064764638, ss4331367372, ss5499798134, ss5786445009	NC_000019.10:40848940:AGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3702784516	NC_000019.10:40848944:AGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss104807062	NT_011109.16:13623063:AGAGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss328033430, ss552626535	NC_000019.8:46046685:AGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
76604813, ss1378156616, ss3743046272, ss3788533421, ss3793443415, ss3798330236, ss5227798786, ss5840561322, ss5981054184	NC_000019.9:41354845:AGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss1710792561, ss1710792566	NC_000019.9:41354851:AGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3821322030, ss4331367371, ss5499798135, ss5786445012, ss5852293693	NC_000019.10:40848940:AGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3702784515	NC_000019.10:40848946:AGAG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3743046271, ss3793443416, ss5227798787, ss5840561323	NC_000019.9:41354845:AG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
	NC_000019.9:41354849:AG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367370, ss5499798136, ss5786445013	NC_000019.10:40848940:AG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3702784514	NC_000019.10:40848948:AG:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3650919794	NC_000019.10:40848955:GA:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss95728915	NT_011109.16:13623098:GA:	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss5227798783	NC_000019.9:41354845::AG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367360, ss5307276228, ss5786445010	NC_000019.10:40848940::AG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss5227798784	NC_000019.9:41354845::AGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367361, ss5786445014	NC_000019.10:40848940::AGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3702784513	NC_000019.10:40848950::AGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367362	NC_000019.10:40848940::AGAGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367363	NC_000019.10:40848940::AGAGAGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367364	NC_000019.10:40848940::AGAGAGAGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
11317217179	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367365	NC_000019.10:40848940::AGAGAGAGAGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367366	NC_000019.10:40848940::AGAGAGAGAGA… NC_000019.10:40848940::AGAGAGAGAGAGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367367	NC_000019.10:40848940::AGAGAGAGAGA… NC_000019.10:40848940::AGAGAGAGAGAGAGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4331367368	NC_000019.10:40848940::AGAGAGAGAGA… NC_000019.10:40848940::AGAGAGAGAGAGAGAGAG	NC_000019.10:40848940:AGAGAGAGAGAG… NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(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 rs67032351

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs67032351