rs1060502392

Orientation

plus

Stabilized

plus

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

Make rs1060502392(-;-)

Make rs1060502392(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32340929

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502392
dbSNP (classic)	rs1060502392
ClinGen	rs1060502392
ebi	rs1060502392
HLI	rs1060502392
Exac	rs1060502392
Gnomad	rs1060502392
Varsome	rs1060502392
LitVar	rs1060502392
Map	rs1060502392
PheGenI	rs1060502392
Biobank	rs1060502392
1000 genomes	rs1060502392
hgdp	rs1060502392
ensembl	rs1060502392
geneview	rs1060502392
scholar	rs1060502392
google	rs1060502392
pharmgkb	rs1060502392
gwascentral	rs1060502392
openSNP	rs1060502392
23andMe	rs1060502392
SNPshot	rs1060502392
SNPdbe	rs1060502392
MSV3d	rs1060502392
GWAS Ctlg	rs1060502392

Max Magnitude

0

ClinVar
Risk	rs1060502392(-;-)
Alt	rs1060502392(-;-)
Reference	Rs1060502392(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.32915066delA
CLNSRC
CLNACC	RCV000475177.1,