rs431825319

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs431825319(C;G)

Make rs431825319(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32338709

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs431825319
dbSNP (classic)	rs431825319
ClinGen	rs431825319
ebi	rs431825319
HLI	rs431825319
Exac	rs431825319
Gnomad	rs431825319
Varsome	rs431825319
LitVar	rs431825319
Map	rs431825319
PheGenI	rs431825319
Biobank	rs431825319
1000 genomes	rs431825319
hgdp	rs431825319
ensembl	rs431825319
geneview	rs431825319
scholar	rs431825319
google	rs431825319
pharmgkb	rs431825319
gwascentral	rs431825319
openSNP	rs431825319
23andMe	rs431825319
SNPshot	rs431825319
SNPdbe	rs431825319
MSV3d	rs431825319
GWAS Ctlg	rs431825319

Max Magnitude

0

ClinVar
Risk	rs431825319(G;G) rs431825319(T;T)
Alt	rs431825319(G;G) rs431825319(T;T)
Reference	Rs431825319(C;C)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32912846C>G; NC_000013.10:g.32912846C>T
CLNSRC
CLNACC	RCV000082927.2, RCV000213089.1, RCV000423930.1,