rs1060502426

Orientation

plus

Stabilized

plus

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

Make rs1060502426(-;-)

Make rs1060502426(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32338628

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502426
dbSNP (classic)	rs1060502426
ClinGen	rs1060502426
ebi	rs1060502426
HLI	rs1060502426
Exac	rs1060502426
Gnomad	rs1060502426
Varsome	rs1060502426
LitVar	rs1060502426
Map	rs1060502426
PheGenI	rs1060502426
Biobank	rs1060502426
1000 genomes	rs1060502426
hgdp	rs1060502426
ensembl	rs1060502426
geneview	rs1060502426
scholar	rs1060502426
google	rs1060502426
pharmgkb	rs1060502426
gwascentral	rs1060502426
openSNP	rs1060502426
23andMe	rs1060502426
SNPshot	rs1060502426
SNPdbe	rs1060502426
MSV3d	rs1060502426
GWAS Ctlg	rs1060502426

Max Magnitude

0

ClinVar
Risk	rs1060502426(-;-)
Alt	rs1060502426(-;-)
Reference	Rs1060502426(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.32912765delG
CLNSRC
CLNACC	RCV000471947.1,