rs1060502433

Orientation

plus

Stabilized

plus

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

Make rs1060502433(A;A)

Make rs1060502433(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32357846

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502433
dbSNP (classic)	rs1060502433
ClinGen	rs1060502433
ebi	rs1060502433
HLI	rs1060502433
Exac	rs1060502433
Gnomad	rs1060502433
Varsome	rs1060502433
LitVar	rs1060502433
Map	rs1060502433
PheGenI	rs1060502433
Biobank	rs1060502433
1000 genomes	rs1060502433
hgdp	rs1060502433
ensembl	rs1060502433
geneview	rs1060502433
scholar	rs1060502433
google	rs1060502433
pharmgkb	rs1060502433
gwascentral	rs1060502433
openSNP	rs1060502433
23andMe	rs1060502433
SNPshot	rs1060502433
SNPdbe	rs1060502433
MSV3d	rs1060502433
GWAS Ctlg	rs1060502433

Max Magnitude

0

ClinVar
Risk	rs1060502433(A;A)
Alt	rs1060502433(A;A)
Reference	Rs1060502433(G;G)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32931983G>A
CLNSRC
CLNACC	RCV000472083.1,