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rs1060502633

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502633(C;T)
Make rs1060502633(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31478129
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502633
dbSNP (old)rs1060502633
ClinGenrs1060502633
ebirs1060502633
HLIrs1060502633
Exacrs1060502633
Gnomadrs1060502633
Varsomers1060502633
Maprs1060502633
PheGenIrs1060502633
Biobankrs1060502633
1000 genomesrs1060502633
hgdprs1060502633
ensemblrs1060502633
gopubmedrs1060502633
geneviewrs1060502633
scholarrs1060502633
googlers1060502633
pharmgkbrs1060502633
gwascentralrs1060502633
openSNPrs1060502633
23andMers1060502633
23andMe allrs1060502633
SNPshotrs1060502633
SNPdbers1060502633
MSV3drs1060502633
GWAS Ctlgrs1060502633
Max Magnitude0
ClinVar
Risk rs1060502633(T;T)
Alt rs1060502633(T;T)
Reference Rs1060502633(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31496246G>A
CLNSRC
CLNACC RCV000470018.1,