rs397508066

Orientation

plus

Stabilized

plus

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

Make rs397508066(-;AA)

Make rs397508066(AA;AA)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332472

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508066
dbSNP (classic)	rs397508066
ClinGen	rs397508066
ebi	rs397508066
HLI	rs397508066
Exac	rs397508066
Gnomad	rs397508066
Varsome	rs397508066
LitVar	rs397508066
Map	rs397508066
PheGenI	rs397508066
Biobank	rs397508066
1000 genomes	rs397508066
hgdp	rs397508066
ensembl	rs397508066
geneview	rs397508066
scholar	rs397508066
google	rs397508066
pharmgkb	rs397508066
gwascentral	rs397508066
openSNP	rs397508066
23andMe	rs397508066
SNPshot	rs397508066
SNPdbe	rs397508066
MSV3d	rs397508066
GWAS Ctlg	rs397508066

Max Magnitude

6

ClinVar
Risk	rs397508066(A;A) rs397508066(AA;AA)
Alt	rs397508066(A;A) rs397508066(AA;AA)
Reference	Rs397508066(-;-)
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.32906608_32906609dupAA; NC_000013.10:g.32906609dupA
CLNSRC	ClinVar
CLNACC	RCV000045922.2, RCV000045924.2, RCV000241048.2,