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rs1060502636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502636(A;A)
Make rs1060502636(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32518098
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502636
dbSNP (old)rs1060502636
ClinGenrs1060502636
ebirs1060502636
HLIrs1060502636
Exacrs1060502636
Gnomadrs1060502636
Varsomers1060502636
Maprs1060502636
PheGenIrs1060502636
Biobankrs1060502636
1000 genomesrs1060502636
hgdprs1060502636
ensemblrs1060502636
gopubmedrs1060502636
geneviewrs1060502636
scholarrs1060502636
googlers1060502636
pharmgkbrs1060502636
gwascentralrs1060502636
openSNPrs1060502636
23andMers1060502636
23andMe allrs1060502636
SNPshotrs1060502636
SNPdbers1060502636
MSV3drs1060502636
GWAS Ctlgrs1060502636
Max Magnitude0
ClinVar
Risk rs1060502636(A;A)
Alt rs1060502636(A;A)
Reference Rs1060502636(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32536215C>T
CLNSRC
CLNACC RCV000458271.1,