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rs1060502623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502623(A;T)
Make rs1060502623(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32343226
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502623
dbSNP (old)rs1060502623
ClinGenrs1060502623
ebirs1060502623
HLIrs1060502623
Exacrs1060502623
Gnomadrs1060502623
Varsomers1060502623
LitVarrs1060502623
Maprs1060502623
PheGenIrs1060502623
Biobankrs1060502623
1000 genomesrs1060502623
hgdprs1060502623
ensemblrs1060502623
gopubmedrs1060502623
geneviewrs1060502623
scholarrs1060502623
googlers1060502623
pharmgkbrs1060502623
gwascentralrs1060502623
openSNPrs1060502623
23andMers1060502623
23andMe allrs1060502623
SNPshotrs1060502623
SNPdbers1060502623
MSV3drs1060502623
GWAS Ctlgrs1060502623
Max Magnitude0
ClinVar
Risk rs1060502623(T;T)
Alt rs1060502623(T;T)
Reference Rs1060502623(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32361343T>A
CLNSRC
CLNACC RCV000457870.1,