rs397507332

Orientation

plus

Stabilized

plus

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

Make rs397507332(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338769

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507332
dbSNP (classic)	rs397507332
ClinGen	rs397507332
ebi	rs397507332
HLI	rs397507332
Exac	rs397507332
Gnomad	rs397507332
Varsome	rs397507332
LitVar	rs397507332
Map	rs397507332
PheGenI	rs397507332
Biobank	rs397507332
1000 genomes	rs397507332
hgdp	rs397507332
ensembl	rs397507332
geneview	rs397507332
scholar	rs397507332
google	rs397507332
pharmgkb	rs397507332
gwascentral	rs397507332
openSNP	rs397507332
23andMe	rs397507332
SNPshot	rs397507332
SNPdbe	rs397507332
MSV3d	rs397507332
GWAS Ctlg	rs397507332

Max Magnitude

6

ClinVar
Risk	rs397507332(-;-)
Alt	rs397507332(-;-)
Reference	Rs397507332(AA;AA)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32912906_32912907delAA
CLNSRC	ClinVar
CLNACC	RCV000031482.5, RCV000044409.2,