rs1060502385

Orientation

plus

Stabilized

plus

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

Make rs1060502385(GTA;TT)

Make rs1060502385(TT;TT)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32332376

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502385
dbSNP (classic)	rs1060502385
ClinGen	rs1060502385
ebi	rs1060502385
HLI	rs1060502385
Exac	rs1060502385
Gnomad	rs1060502385
Varsome	rs1060502385
LitVar	rs1060502385
Map	rs1060502385
PheGenI	rs1060502385
Biobank	rs1060502385
1000 genomes	rs1060502385
hgdp	rs1060502385
ensembl	rs1060502385
geneview	rs1060502385
scholar	rs1060502385
google	rs1060502385
pharmgkb	rs1060502385
gwascentral	rs1060502385
openSNP	rs1060502385
23andMe	rs1060502385
SNPshot	rs1060502385
SNPdbe	rs1060502385
MSV3d	rs1060502385
GWAS Ctlg	rs1060502385

Max Magnitude

0

ClinVar
Risk	rs1060502385(TT;TT)
Alt	rs1060502385(TT;TT)
Reference	Rs1060502385(GTA;GTA)
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.32906513_32906515delGTAinsTT
CLNSRC
CLNACC	RCV000470864.1,