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rs1060502659

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs1060502659(-;-)
Make rs1060502659(-;AC)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31875217
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502659
dbSNP (old)rs1060502659
ClinGenrs1060502659
ebirs1060502659
HLIrs1060502659
Exacrs1060502659
Gnomadrs1060502659
Varsomers1060502659
Maprs1060502659
PheGenIrs1060502659
Biobankrs1060502659
1000 genomesrs1060502659
hgdprs1060502659
ensemblrs1060502659
gopubmedrs1060502659
geneviewrs1060502659
scholarrs1060502659
googlers1060502659
pharmgkbrs1060502659
gwascentralrs1060502659
openSNPrs1060502659
23andMers1060502659
23andMe allrs1060502659
SNPshotrs1060502659
SNPdbers1060502659
MSV3drs1060502659
GWAS Ctlgrs1060502659
Max Magnitude0
ClinVar
Risk rs1060502659(-;-)
Alt rs1060502659(-;-)
Reference Rs1060502659(AC;AC)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31893334_31893335delGT
CLNSRC
CLNACC RCV000456686.1,