rs1060502437

Orientation

plus

Stabilized

plus

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

Make rs1060502437(-;-)

Make rs1060502437(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32336829

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502437
dbSNP (classic)	rs1060502437
ClinGen	rs1060502437
ebi	rs1060502437
HLI	rs1060502437
Exac	rs1060502437
Gnomad	rs1060502437
Varsome	rs1060502437
LitVar	rs1060502437
Map	rs1060502437
PheGenI	rs1060502437
Biobank	rs1060502437
1000 genomes	rs1060502437
hgdp	rs1060502437
ensembl	rs1060502437
geneview	rs1060502437
scholar	rs1060502437
google	rs1060502437
pharmgkb	rs1060502437
gwascentral	rs1060502437
openSNP	rs1060502437
23andMe	rs1060502437
SNPshot	rs1060502437
SNPdbe	rs1060502437
MSV3d	rs1060502437
GWAS Ctlg	rs1060502437

Max Magnitude

0

ClinVar
Risk	rs1060502437(-;-)
Alt	rs1060502437(-;-)
Reference	Rs1060502437(A;A)
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.32910966delA
CLNSRC
CLNACC	RCV000471125.1,