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rs1060502621

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502621(C;T)
Make rs1060502621(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31627681
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502621
dbSNP (old)rs1060502621
ClinGenrs1060502621
ebirs1060502621
HLIrs1060502621
Exacrs1060502621
Gnomadrs1060502621
Varsomers1060502621
Maprs1060502621
PheGenIrs1060502621
Biobankrs1060502621
1000 genomesrs1060502621
hgdprs1060502621
ensemblrs1060502621
gopubmedrs1060502621
geneviewrs1060502621
scholarrs1060502621
googlers1060502621
pharmgkbrs1060502621
gwascentralrs1060502621
openSNPrs1060502621
23andMers1060502621
23andMe allrs1060502621
SNPshotrs1060502621
SNPdbers1060502621
MSV3drs1060502621
GWAS Ctlgrs1060502621
Max Magnitude0
ClinVar
Risk rs1060502621(T;T)
Alt rs1060502621(T;T)
Reference Rs1060502621(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31645798G>A
CLNSRC
CLNACC RCV000477000.1,