rs397508012

Orientation

plus

Stabilized

plus

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

Make rs397508012(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379383

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508012
dbSNP (classic)	rs397508012
ClinGen	rs397508012
ebi	rs397508012
HLI	rs397508012
Exac	rs397508012
Gnomad	rs397508012
Varsome	rs397508012
LitVar	rs397508012
Map	rs397508012
PheGenI	rs397508012
Biobank	rs397508012
1000 genomes	rs397508012
hgdp	rs397508012
ensembl	rs397508012
geneview	rs397508012
scholar	rs397508012
google	rs397508012
pharmgkb	rs397508012
gwascentral	rs397508012
openSNP	rs397508012
23andMe	rs397508012
SNPshot	rs397508012
SNPdbe	rs397508012
MSV3d	rs397508012
GWAS Ctlg	rs397508012

Max Magnitude

6

ClinVar
Risk	rs397508012(T;T)
Alt	rs397508012(T;T)
Reference	Rs397508012(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.32953520C>T
CLNSRC	ClinVar
CLNACC	RCV000045635.2, RCV000256787.2,