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rs1060502615

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502615(A;T)
Make rs1060502615(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32454659
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502615
dbSNP (old)rs1060502615
ClinGenrs1060502615
ebirs1060502615
HLIrs1060502615
Exacrs1060502615
Gnomadrs1060502615
Varsomers1060502615
Maprs1060502615
PheGenIrs1060502615
Biobankrs1060502615
1000 genomesrs1060502615
hgdprs1060502615
ensemblrs1060502615
gopubmedrs1060502615
geneviewrs1060502615
scholarrs1060502615
googlers1060502615
pharmgkbrs1060502615
gwascentralrs1060502615
openSNPrs1060502615
23andMers1060502615
23andMe allrs1060502615
SNPshotrs1060502615
SNPdbers1060502615
MSV3drs1060502615
GWAS Ctlgrs1060502615
Max Magnitude0
ClinVar
Risk rs1060502615(T;T)
Alt rs1060502615(T;T)
Reference Rs1060502615(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32472776T>A
CLNSRC
CLNACC RCV000473410.1,