rs1060502644

Orientation

minus

Stabilized

minus

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

Make rs1060502644(A;A)

Make rs1060502644(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32645052

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502644
dbSNP (classic)	rs1060502644
ClinGen	rs1060502644
ebi	rs1060502644
HLI	rs1060502644
Exac	rs1060502644
Gnomad	rs1060502644
Varsome	rs1060502644
LitVar	rs1060502644
Map	rs1060502644
PheGenI	rs1060502644
Biobank	rs1060502644
1000 genomes	rs1060502644
hgdp	rs1060502644
ensembl	rs1060502644
geneview	rs1060502644
scholar	rs1060502644
google	rs1060502644
pharmgkb	rs1060502644
gwascentral	rs1060502644
openSNP	rs1060502644
23andMe	rs1060502644
SNPshot	rs1060502644
SNPdbe	rs1060502644
MSV3d	rs1060502644
GWAS Ctlg	rs1060502644

Max Magnitude

0

ClinVar
Risk	rs1060502644(A;A)
Alt	rs1060502644(A;A)
Reference	Rs1060502644(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32663169C>T
CLNSRC
CLNACC	RCV000475363.1,