rs1060502478

Orientation

plus

Stabilized

plus

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

Make rs1060502478(-;-)

Make rs1060502478(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32362536

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502478
dbSNP (classic)	rs1060502478
ClinGen	rs1060502478
ebi	rs1060502478
HLI	rs1060502478
Exac	rs1060502478
Gnomad	rs1060502478
Varsome	rs1060502478
LitVar	rs1060502478
Map	rs1060502478
PheGenI	rs1060502478
Biobank	rs1060502478
1000 genomes	rs1060502478
hgdp	rs1060502478
ensembl	rs1060502478
geneview	rs1060502478
scholar	rs1060502478
google	rs1060502478
pharmgkb	rs1060502478
gwascentral	rs1060502478
openSNP	rs1060502478
23andMe	rs1060502478
SNPshot	rs1060502478
SNPdbe	rs1060502478
MSV3d	rs1060502478
GWAS Ctlg	rs1060502478

Max Magnitude

0

ClinVar
Risk	rs1060502478(-;-)
Alt	rs1060502478(-;-)
Reference	Rs1060502478(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.32936673delA
CLNSRC
CLNACC	RCV000470903.1,