rs1060502475

Orientation

plus

Stabilized

plus

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

Make rs1060502475(-;-)

Make rs1060502475(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32337432

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502475
dbSNP (classic)	rs1060502475
ClinGen	rs1060502475
ebi	rs1060502475
HLI	rs1060502475
Exac	rs1060502475
Gnomad	rs1060502475
Varsome	rs1060502475
LitVar	rs1060502475
Map	rs1060502475
PheGenI	rs1060502475
Biobank	rs1060502475
1000 genomes	rs1060502475
hgdp	rs1060502475
ensembl	rs1060502475
geneview	rs1060502475
scholar	rs1060502475
google	rs1060502475
pharmgkb	rs1060502475
gwascentral	rs1060502475
openSNP	rs1060502475
23andMe	rs1060502475
SNPshot	rs1060502475
SNPdbe	rs1060502475
MSV3d	rs1060502475
GWAS Ctlg	rs1060502475

Max Magnitude

0

ClinVar
Risk	rs1060502475(-;-)
Alt	rs1060502475(-;-)
Reference	Rs1060502475(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.32911569delA
CLNSRC
CLNACC	RCV000468393.1,