rs1060502376

Orientation

plus

Stabilized

plus

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

Make rs1060502376(G;T)

Make rs1060502376(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32319076

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502376
dbSNP (classic)	rs1060502376
ClinGen	rs1060502376
ebi	rs1060502376
HLI	rs1060502376
Exac	rs1060502376
Gnomad	rs1060502376
Varsome	rs1060502376
LitVar	rs1060502376
Map	rs1060502376
PheGenI	rs1060502376
Biobank	rs1060502376
1000 genomes	rs1060502376
hgdp	rs1060502376
ensembl	rs1060502376
geneview	rs1060502376
scholar	rs1060502376
google	rs1060502376
pharmgkb	rs1060502376
gwascentral	rs1060502376
openSNP	rs1060502376
23andMe	rs1060502376
SNPshot	rs1060502376
SNPdbe	rs1060502376
MSV3d	rs1060502376
GWAS Ctlg	rs1060502376

Max Magnitude

0

ClinVar
Risk	rs1060502376(T;T)
Alt	rs1060502376(T;T)
Reference	Rs1060502376(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome not specified
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome not specified
Reversed	0
HGVS	NC_000013.10:g.32893213G>T
CLNSRC
CLNACC	RCV000458301.1, RCV000483572.1,