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rs1060502648

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502648(-;-)
Make rs1060502648(-;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31209627
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502648
dbSNP (old)rs1060502648
ClinGenrs1060502648
ebirs1060502648
HLIrs1060502648
Exacrs1060502648
Gnomadrs1060502648
Varsomers1060502648
Maprs1060502648
PheGenIrs1060502648
Biobankrs1060502648
1000 genomesrs1060502648
hgdprs1060502648
ensemblrs1060502648
gopubmedrs1060502648
geneviewrs1060502648
scholarrs1060502648
googlers1060502648
pharmgkbrs1060502648
gwascentralrs1060502648
openSNPrs1060502648
23andMers1060502648
23andMe allrs1060502648
SNPshotrs1060502648
SNPdbers1060502648
MSV3drs1060502648
GWAS Ctlgrs1060502648
Max Magnitude0
ClinVar
Risk rs1060502648(-;-)
Alt rs1060502648(-;-)
Reference Rs1060502648(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31227744delA
CLNSRC
CLNACC RCV000457661.1,