rs397508025

Orientation

plus

Stabilized

plus

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

Make rs397508025(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379774

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508025
dbSNP (classic)	rs397508025
ClinGen	rs397508025
ebi	rs397508025
HLI	rs397508025
Exac	rs397508025
Gnomad	rs397508025
Varsome	rs397508025
LitVar	rs397508025
Map	rs397508025
PheGenI	rs397508025
Biobank	rs397508025
1000 genomes	rs397508025
hgdp	rs397508025
ensembl	rs397508025
geneview	rs397508025
scholar	rs397508025
google	rs397508025
pharmgkb	rs397508025
gwascentral	rs397508025
openSNP	rs397508025
23andMe	rs397508025
SNPshot	rs397508025
SNPdbe	rs397508025
MSV3d	rs397508025
GWAS Ctlg	rs397508025

Max Magnitude

6

ClinVar
Risk	rs397508025(A;A) rs397508025(G;G)
Alt	rs397508025(A;A) rs397508025(G;G)
Reference	Rs397508025(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32953911C>A; NC_000013.10:g.32953911C>G
CLNSRC	ClinVar
CLNACC	RCV000045677.2, RCV000256867.2, RCV000160161.2, RCV000221983.1, RCV000241294.1,