rs397507938

Orientation

plus

Stabilized

plus

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

Make rs397507938(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32357929

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507938
dbSNP (classic)	rs397507938
ClinGen	rs397507938
ebi	rs397507938
HLI	rs397507938
Exac	rs397507938
Gnomad	rs397507938
Varsome	rs397507938
LitVar	rs397507938
Map	rs397507938
PheGenI	rs397507938
Biobank	rs397507938
1000 genomes	rs397507938
hgdp	rs397507938
ensembl	rs397507938
geneview	rs397507938
scholar	rs397507938
google	rs397507938
pharmgkb	rs397507938
gwascentral	rs397507938
openSNP	rs397507938
23andMe	rs397507938
SNPshot	rs397507938
SNPdbe	rs397507938
MSV3d	rs397507938
GWAS Ctlg	rs397507938

Max Magnitude

6

ClinVar
Risk	rs397507938(C;C)
Alt	rs397507938(C;C)
Reference	Rs397507938(G;G)
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.32932066G>C
CLNSRC	ClinVar
CLNACC	RCV000045318.2, RCV000258178.1,