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rs1060502641

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502641(C;C)
Make rs1060502641(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31968337
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502641
dbSNP (old)rs1060502641
ClinGenrs1060502641
ebirs1060502641
HLIrs1060502641
Exacrs1060502641
Gnomadrs1060502641
Varsomers1060502641
Maprs1060502641
PheGenIrs1060502641
Biobankrs1060502641
1000 genomesrs1060502641
hgdprs1060502641
ensemblrs1060502641
gopubmedrs1060502641
geneviewrs1060502641
scholarrs1060502641
googlers1060502641
pharmgkbrs1060502641
gwascentralrs1060502641
openSNPrs1060502641
23andMers1060502641
23andMe allrs1060502641
SNPshotrs1060502641
SNPdbers1060502641
MSV3drs1060502641
GWAS Ctlgrs1060502641
Max Magnitude0
ClinVar
Risk rs1060502641(C;C)
Alt rs1060502641(C;C)
Reference Rs1060502641(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31986454A>G
CLNSRC
CLNACC RCV000473580.1,