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rs1060502627

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502627(A;A)
Make rs1060502627(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32518024
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502627
dbSNP (old)rs1060502627
ClinGenrs1060502627
ebirs1060502627
HLIrs1060502627
Exacrs1060502627
Gnomadrs1060502627
Varsomers1060502627
Maprs1060502627
PheGenIrs1060502627
Biobankrs1060502627
1000 genomesrs1060502627
hgdprs1060502627
ensemblrs1060502627
gopubmedrs1060502627
geneviewrs1060502627
scholarrs1060502627
googlers1060502627
pharmgkbrs1060502627
gwascentralrs1060502627
openSNPrs1060502627
23andMers1060502627
23andMe allrs1060502627
SNPshotrs1060502627
SNPdbers1060502627
MSV3drs1060502627
GWAS Ctlgrs1060502627
Max Magnitude0
ClinVar
Risk rs1060502627(A;A)
Alt rs1060502627(A;A)
Reference Rs1060502627(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32536141A>T
CLNSRC
CLNACC RCV000472980.1,