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rs1060502626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502626(A;A)
Make rs1060502626(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31147274
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502626
dbSNP (old)rs1060502626
ClinGenrs1060502626
ebirs1060502626
HLIrs1060502626
Exacrs1060502626
Gnomadrs1060502626
Varsomers1060502626
Maprs1060502626
PheGenIrs1060502626
Biobankrs1060502626
1000 genomesrs1060502626
hgdprs1060502626
ensemblrs1060502626
gopubmedrs1060502626
geneviewrs1060502626
scholarrs1060502626
googlers1060502626
pharmgkbrs1060502626
gwascentralrs1060502626
openSNPrs1060502626
23andMers1060502626
23andMe allrs1060502626
SNPshotrs1060502626
SNPdbers1060502626
MSV3drs1060502626
GWAS Ctlgrs1060502626
Max Magnitude0
ClinVar
Risk rs1060502626(A;A)
Alt rs1060502626(A;A)
Reference Rs1060502626(G;G)
Significance Probable-Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31165391C>T
CLNSRC
CLNACC RCV000464915.1,