rs397507662

Orientation

plus

Stabilized

plus

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

Make rs397507662(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337638

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507662
dbSNP (classic)	rs397507662
ClinGen	rs397507662
ebi	rs397507662
HLI	rs397507662
Exac	rs397507662
Gnomad	rs397507662
Varsome	rs397507662
LitVar	rs397507662
Map	rs397507662
PheGenI	rs397507662
Biobank	rs397507662
1000 genomes	rs397507662
hgdp	rs397507662
ensembl	rs397507662
geneview	rs397507662
scholar	rs397507662
google	rs397507662
pharmgkb	rs397507662
gwascentral	rs397507662
openSNP	rs397507662
23andMe	rs397507662
SNPshot	rs397507662
SNPdbe	rs397507662
MSV3d	rs397507662
GWAS Ctlg	rs397507662

Max Magnitude

6

ClinVar
Risk	rs397507662(T;T)
Alt	rs397507662(T;T)
Reference	Rs397507662(C;C)
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.32911775C>T
CLNSRC	ClinVar
CLNACC	RCV000044170.2, RCV000162053.3,