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rs1060502634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502634(A;A)
Make rs1060502634(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32644963
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502634
dbSNP (old)rs1060502634
ClinGenrs1060502634
ebirs1060502634
HLIrs1060502634
Exacrs1060502634
Gnomadrs1060502634
Varsomers1060502634
Maprs1060502634
PheGenIrs1060502634
Biobankrs1060502634
1000 genomesrs1060502634
hgdprs1060502634
ensemblrs1060502634
gopubmedrs1060502634
geneviewrs1060502634
scholarrs1060502634
googlers1060502634
pharmgkbrs1060502634
gwascentralrs1060502634
openSNPrs1060502634
23andMers1060502634
23andMe allrs1060502634
SNPshotrs1060502634
SNPdbers1060502634
MSV3drs1060502634
GWAS Ctlgrs1060502634
Max Magnitude0
ClinVar
Risk rs1060502634(A;A)
Alt rs1060502634(A;A)
Reference Rs1060502634(G;G)
Significance Probable-Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32663080C>T
CLNSRC
CLNACC RCV000458031.1,