rs1060502465

Orientation

plus

Stabilized

plus

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

Make rs1060502465(-;-)

Make rs1060502465(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32326504

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502465
dbSNP (classic)	rs1060502465
ClinGen	rs1060502465
ebi	rs1060502465
HLI	rs1060502465
Exac	rs1060502465
Gnomad	rs1060502465
Varsome	rs1060502465
LitVar	rs1060502465
Map	rs1060502465
PheGenI	rs1060502465
Biobank	rs1060502465
1000 genomes	rs1060502465
hgdp	rs1060502465
ensembl	rs1060502465
geneview	rs1060502465
scholar	rs1060502465
google	rs1060502465
pharmgkb	rs1060502465
gwascentral	rs1060502465
openSNP	rs1060502465
23andMe	rs1060502465
SNPshot	rs1060502465
SNPdbe	rs1060502465
MSV3d	rs1060502465
GWAS Ctlg	rs1060502465

Max Magnitude

0

ClinVar
Risk	rs1060502465(-;-)
Alt	rs1060502465(-;-)
Reference	Rs1060502465(T;T)
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.32900641delT
CLNSRC
CLNACC	RCV000476820.1,