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rs1060502645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502645(G;T)
Make rs1060502645(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32365187
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502645
dbSNP (old)rs1060502645
ClinGenrs1060502645
ebirs1060502645
HLIrs1060502645
Exacrs1060502645
Gnomadrs1060502645
Varsomers1060502645
Maprs1060502645
PheGenIrs1060502645
Biobankrs1060502645
1000 genomesrs1060502645
hgdprs1060502645
ensemblrs1060502645
gopubmedrs1060502645
geneviewrs1060502645
scholarrs1060502645
googlers1060502645
pharmgkbrs1060502645
gwascentralrs1060502645
openSNPrs1060502645
23andMers1060502645
23andMe allrs1060502645
SNPshotrs1060502645
SNPdbers1060502645
MSV3drs1060502645
GWAS Ctlgrs1060502645
Max Magnitude0
ClinVar
Risk rs1060502645(T;T)
Alt rs1060502645(T;T)
Reference Rs1060502645(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32383304C>A
CLNSRC
CLNACC RCV000463648.1,