rs397507908

Orientation

plus

Stabilized

plus

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

Make rs397507908(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32355114

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507908
dbSNP (classic)	rs397507908
ClinGen	rs397507908
ebi	rs397507908
HLI	rs397507908
Exac	rs397507908
Gnomad	rs397507908
Varsome	rs397507908
LitVar	rs397507908
Map	rs397507908
PheGenI	rs397507908
Biobank	rs397507908
1000 genomes	rs397507908
hgdp	rs397507908
ensembl	rs397507908
geneview	rs397507908
scholar	rs397507908
google	rs397507908
pharmgkb	rs397507908
gwascentral	rs397507908
openSNP	rs397507908
23andMe	rs397507908
SNPshot	rs397507908
SNPdbe	rs397507908
MSV3d	rs397507908
GWAS Ctlg	rs397507908

Max Magnitude

6

ClinVar
Risk	rs397507908(T;T)
Alt	rs397507908(T;T)
Reference	Rs397507908(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.32929251C>T
CLNSRC	ClinVar
CLNACC	RCV000045179.2, RCV000241497.2,