rs1060502430

Orientation

plus

Stabilized

plus

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

Make rs1060502430(-;-)

Make rs1060502430(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32340008

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502430
dbSNP (classic)	rs1060502430
ClinGen	rs1060502430
ebi	rs1060502430
HLI	rs1060502430
Exac	rs1060502430
Gnomad	rs1060502430
Varsome	rs1060502430
LitVar	rs1060502430
Map	rs1060502430
PheGenI	rs1060502430
Biobank	rs1060502430
1000 genomes	rs1060502430
hgdp	rs1060502430
ensembl	rs1060502430
geneview	rs1060502430
scholar	rs1060502430
google	rs1060502430
pharmgkb	rs1060502430
gwascentral	rs1060502430
openSNP	rs1060502430
23andMe	rs1060502430
SNPshot	rs1060502430
SNPdbe	rs1060502430
MSV3d	rs1060502430
GWAS Ctlg	rs1060502430

Max Magnitude

0

ClinVar
Risk	rs1060502430(-;-)
Alt	rs1060502430(-;-)
Reference	Rs1060502430(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.32914145delT
CLNSRC
CLNACC	RCV000476395.1,