rs1060502625

Orientation

minus

Stabilized

minus

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

Make rs1060502625(-;-)

Make rs1060502625(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31147347

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502625
dbSNP (classic)	rs1060502625
ClinGen	rs1060502625
ebi	rs1060502625
HLI	rs1060502625
Exac	rs1060502625
Gnomad	rs1060502625
Varsome	rs1060502625
LitVar	rs1060502625
Map	rs1060502625
PheGenI	rs1060502625
Biobank	rs1060502625
1000 genomes	rs1060502625
hgdp	rs1060502625
ensembl	rs1060502625
geneview	rs1060502625
scholar	rs1060502625
google	rs1060502625
pharmgkb	rs1060502625
gwascentral	rs1060502625
openSNP	rs1060502625
23andMe	rs1060502625
SNPshot	rs1060502625
SNPdbe	rs1060502625
MSV3d	rs1060502625
GWAS Ctlg	rs1060502625

Max Magnitude

0

ClinVar
Risk	rs1060502625(-;-)
Alt	rs1060502625(-;-)
Reference	Rs1060502625(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31165464delC
CLNSRC
CLNACC	RCV000473878.1,