rs1060502471

Orientation

plus

Stabilized

plus

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

Make rs1060502471(-;-)

Make rs1060502471(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32371075

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502471
dbSNP (classic)	rs1060502471
ClinGen	rs1060502471
ebi	rs1060502471
HLI	rs1060502471
Exac	rs1060502471
Gnomad	rs1060502471
Varsome	rs1060502471
LitVar	rs1060502471
Map	rs1060502471
PheGenI	rs1060502471
Biobank	rs1060502471
1000 genomes	rs1060502471
hgdp	rs1060502471
ensembl	rs1060502471
geneview	rs1060502471
scholar	rs1060502471
google	rs1060502471
pharmgkb	rs1060502471
gwascentral	rs1060502471
openSNP	rs1060502471
23andMe	rs1060502471
SNPshot	rs1060502471
SNPdbe	rs1060502471
MSV3d	rs1060502471
GWAS Ctlg	rs1060502471

Max Magnitude

0

ClinVar
Risk	rs1060502471(-;-)
Alt	rs1060502471(-;-)
Reference	Rs1060502471(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.32945212delT
CLNSRC
CLNACC	RCV000470808.1,