rs1060502455

Orientation

plus

Stabilized

plus

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

Make rs1060502455(-;-)

Make rs1060502455(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32336337

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502455
dbSNP (classic)	rs1060502455
ClinGen	rs1060502455
ebi	rs1060502455
HLI	rs1060502455
Exac	rs1060502455
Gnomad	rs1060502455
Varsome	rs1060502455
LitVar	rs1060502455
Map	rs1060502455
PheGenI	rs1060502455
Biobank	rs1060502455
1000 genomes	rs1060502455
hgdp	rs1060502455
ensembl	rs1060502455
geneview	rs1060502455
scholar	rs1060502455
google	rs1060502455
pharmgkb	rs1060502455
gwascentral	rs1060502455
openSNP	rs1060502455
23andMe	rs1060502455
SNPshot	rs1060502455
SNPdbe	rs1060502455
MSV3d	rs1060502455
GWAS Ctlg	rs1060502455

Max Magnitude

0

ClinVar
Risk	rs1060502455(-;-)
Alt	rs1060502455(-;-)
Reference	Rs1060502455(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.32910474delG
CLNSRC
CLNACC	RCV000458243.1,