rs1060502466

Orientation

plus

Stabilized

plus

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

Make rs1060502466(C;C)

Make rs1060502466(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32336837

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502466
dbSNP (classic)	rs1060502466
ClinGen	rs1060502466
ebi	rs1060502466
HLI	rs1060502466
Exac	rs1060502466
Gnomad	rs1060502466
Varsome	rs1060502466
LitVar	rs1060502466
Map	rs1060502466
PheGenI	rs1060502466
Biobank	rs1060502466
1000 genomes	rs1060502466
hgdp	rs1060502466
ensembl	rs1060502466
geneview	rs1060502466
scholar	rs1060502466
google	rs1060502466
pharmgkb	rs1060502466
gwascentral	rs1060502466
openSNP	rs1060502466
23andMe	rs1060502466
SNPshot	rs1060502466
SNPdbe	rs1060502466
MSV3d	rs1060502466
GWAS Ctlg	rs1060502466

Max Magnitude

0

ClinVar
Risk	rs1060502466(C;C)
Alt	rs1060502466(C;C)
Reference	Rs1060502466(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910974T>C
CLNSRC
CLNACC	RCV000463755.1, RCV000487989.1,