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rs1060502661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502661(C;T)
Make rs1060502661(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32545250
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502661
dbSNP (old)rs1060502661
ClinGenrs1060502661
ebirs1060502661
HLIrs1060502661
Exacrs1060502661
Gnomadrs1060502661
Varsomers1060502661
Maprs1060502661
PheGenIrs1060502661
Biobankrs1060502661
1000 genomesrs1060502661
hgdprs1060502661
ensemblrs1060502661
gopubmedrs1060502661
geneviewrs1060502661
scholarrs1060502661
googlers1060502661
pharmgkbrs1060502661
gwascentralrs1060502661
openSNPrs1060502661
23andMers1060502661
23andMe allrs1060502661
SNPshotrs1060502661
SNPdbers1060502661
MSV3drs1060502661
GWAS Ctlgrs1060502661
Max Magnitude0
ClinVar
Risk rs1060502661(T;T)
Alt rs1060502661(T;T)
Reference Rs1060502661(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32563367G>A
CLNSRC
CLNACC RCV000466434.1,