rs1060502391

Orientation

plus

Stabilized

plus

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

Make rs1060502391(-;-)

Make rs1060502391(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32337331

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502391
dbSNP (classic)	rs1060502391
ClinGen	rs1060502391
ebi	rs1060502391
HLI	rs1060502391
Exac	rs1060502391
Gnomad	rs1060502391
Varsome	rs1060502391
LitVar	rs1060502391
Map	rs1060502391
PheGenI	rs1060502391
Biobank	rs1060502391
1000 genomes	rs1060502391
hgdp	rs1060502391
ensembl	rs1060502391
geneview	rs1060502391
scholar	rs1060502391
google	rs1060502391
pharmgkb	rs1060502391
gwascentral	rs1060502391
openSNP	rs1060502391
23andMe	rs1060502391
SNPshot	rs1060502391
SNPdbe	rs1060502391
MSV3d	rs1060502391
GWAS Ctlg	rs1060502391

Max Magnitude

0

ClinVar
Risk	rs1060502391(-;-)
Alt	rs1060502391(-;-)
Reference	Rs1060502391(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.32911468delA
CLNSRC
CLNACC	RCV000475958.1,