rs397507801

Orientation

plus

Stabilized

plus

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

Make rs397507801(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340094

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507801
dbSNP (classic)	rs397507801
ClinGen	rs397507801
ebi	rs397507801
HLI	rs397507801
Exac	rs397507801
Gnomad	rs397507801
Varsome	rs397507801
LitVar	rs397507801
Map	rs397507801
PheGenI	rs397507801
Biobank	rs397507801
1000 genomes	rs397507801
hgdp	rs397507801
ensembl	rs397507801
geneview	rs397507801
scholar	rs397507801
google	rs397507801
pharmgkb	rs397507801
gwascentral	rs397507801
openSNP	rs397507801
23andMe	rs397507801
SNPshot	rs397507801
SNPdbe	rs397507801
MSV3d	rs397507801
GWAS Ctlg	rs397507801

Max Magnitude

6

ClinVar
Risk	rs397507801(A;A)
Alt	rs397507801(A;A)
Reference	Rs397507801(T;T)
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.32914231T>A
CLNSRC	ClinVar
CLNACC	RCV000044739.2, RCV000241195.1,