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rs1060502643

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502643(A;A)
Make rs1060502643(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32438240
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502643
dbSNP (old)rs1060502643
ClinGenrs1060502643
ebirs1060502643
HLIrs1060502643
Exacrs1060502643
Gnomadrs1060502643
Varsomers1060502643
Maprs1060502643
PheGenIrs1060502643
Biobankrs1060502643
1000 genomesrs1060502643
hgdprs1060502643
ensemblrs1060502643
gopubmedrs1060502643
geneviewrs1060502643
scholarrs1060502643
googlers1060502643
pharmgkbrs1060502643
gwascentralrs1060502643
openSNPrs1060502643
23andMers1060502643
23andMe allrs1060502643
SNPshotrs1060502643
SNPdbers1060502643
MSV3drs1060502643
GWAS Ctlgrs1060502643
Max Magnitude0
ClinVar
Risk rs1060502643(A;A)
Alt rs1060502643(A;A)
Reference Rs1060502643(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32456357C>T
CLNSRC
CLNACC RCV000475286.1,