rs1060502485

Orientation

plus

Stabilized

plus

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

Make rs1060502485(A;A)

Make rs1060502485(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32326100

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502485
dbSNP (classic)	rs1060502485
ClinGen	rs1060502485
ebi	rs1060502485
HLI	rs1060502485
Exac	rs1060502485
Gnomad	rs1060502485
Varsome	rs1060502485
LitVar	rs1060502485
Map	rs1060502485
PheGenI	rs1060502485
Biobank	rs1060502485
1000 genomes	rs1060502485
hgdp	rs1060502485
ensembl	rs1060502485
geneview	rs1060502485
scholar	rs1060502485
google	rs1060502485
pharmgkb	rs1060502485
gwascentral	rs1060502485
openSNP	rs1060502485
23andMe	rs1060502485
SNPshot	rs1060502485
SNPdbe	rs1060502485
MSV3d	rs1060502485
GWAS Ctlg	rs1060502485

Max Magnitude

0

ClinVar
Risk	rs1060502485(A;A)
Alt	rs1060502485(A;A)
Reference	Rs1060502485(G;G)
Significance	Probable-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.32900237G>A
CLNSRC
CLNACC	RCV000470985.1,