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rs1060502653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTAGACCTTT;GTAGACCTTT) 0 common in clinvar
Make rs1060502653(-;-)
Make rs1060502653(-;GTAGACCTTT)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31204113
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502653
dbSNP (old)rs1060502653
ClinGenrs1060502653
ebirs1060502653
HLIrs1060502653
Exacrs1060502653
Gnomadrs1060502653
Varsomers1060502653
Maprs1060502653
PheGenIrs1060502653
Biobankrs1060502653
1000 genomesrs1060502653
hgdprs1060502653
ensemblrs1060502653
gopubmedrs1060502653
geneviewrs1060502653
scholarrs1060502653
googlers1060502653
pharmgkbrs1060502653
gwascentralrs1060502653
openSNPrs1060502653
23andMers1060502653
23andMe allrs1060502653
SNPshotrs1060502653
SNPdbers1060502653
MSV3drs1060502653
GWAS Ctlgrs1060502653
Max Magnitude0
ClinVar
Risk rs1060502653(-;-)
Alt rs1060502653(-;-)
Reference Rs1060502653(GTAGACCTTT;GTAGACCTTT)
Significance Probable-Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31222230_31222239delAAAGGTCTAC
CLNSRC
CLNACC RCV000467852.1,