rs397508031

Merged into

rs80359738

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;G)	6	BRCA2 variant considered pathogenic for breast cancer

Make rs397508031(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332379

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508031
dbSNP (classic)	rs397508031
ClinGen	rs397508031
ebi	rs397508031
HLI	rs397508031
Exac	rs397508031
Gnomad	rs397508031
Varsome	rs397508031
LitVar	rs397508031
Map	rs397508031
PheGenI	rs397508031
Biobank	rs397508031
1000 genomes	rs397508031
hgdp	rs397508031
ensembl	rs397508031
geneview	rs397508031
scholar	rs397508031
google	rs397508031
pharmgkb	rs397508031
gwascentral	rs397508031
openSNP	rs397508031
23andMe	rs397508031
SNPshot	rs397508031
SNPdbe	rs397508031
MSV3d	rs397508031
GWAS Ctlg	rs397508031

Status

Merged into rs80359738

Max Magnitude

6

ClinVar
Risk	rs397508031(G;G)
Alt	rs397508031(G;G)
Reference	Rs397508031(;)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32906516dupG
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045691.2, RCV000112861.2,