rs431825315

Orientation

plus

Stabilized

plus

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

Make rs431825315(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338440

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs431825315
dbSNP (classic)	rs431825315
ClinGen	rs431825315
ebi	rs431825315
HLI	rs431825315
Exac	rs431825315
Gnomad	rs431825315
Varsome	rs431825315
LitVar	rs431825315
Map	rs431825315
PheGenI	rs431825315
Biobank	rs431825315
1000 genomes	rs431825315
hgdp	rs431825315
ensembl	rs431825315
geneview	rs431825315
scholar	rs431825315
google	rs431825315
pharmgkb	rs431825315
gwascentral	rs431825315
openSNP	rs431825315
23andMe	rs431825315
SNPshot	rs431825315
SNPdbe	rs431825315
MSV3d	rs431825315
GWAS Ctlg	rs431825315

Max Magnitude

6

ClinVar
Risk	rs431825315(-;-)
Alt	rs431825315(-;-)
Reference	Rs431825315(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912577delA
CLNSRC	ClinVar
CLNACC	RCV000082923.3,