Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060502644

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502644(A;A)
Make rs1060502644(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32645052
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502644
dbSNP (old)rs1060502644
ClinGenrs1060502644
ebirs1060502644
HLIrs1060502644
Exacrs1060502644
Gnomadrs1060502644
Varsomers1060502644
Maprs1060502644
PheGenIrs1060502644
Biobankrs1060502644
1000 genomesrs1060502644
hgdprs1060502644
ensemblrs1060502644
gopubmedrs1060502644
geneviewrs1060502644
scholarrs1060502644
googlers1060502644
pharmgkbrs1060502644
gwascentralrs1060502644
openSNPrs1060502644
23andMers1060502644
23andMe allrs1060502644
SNPshotrs1060502644
SNPdbers1060502644
MSV3drs1060502644
GWAS Ctlgrs1060502644
Max Magnitude0
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,