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rs1060502639

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502639(C;T)
Make rs1060502639(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32485057
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502639
dbSNP (old)rs1060502639
ClinGenrs1060502639
ebirs1060502639
HLIrs1060502639
Exacrs1060502639
Gnomadrs1060502639
Varsomers1060502639
Maprs1060502639
PheGenIrs1060502639
Biobankrs1060502639
1000 genomesrs1060502639
hgdprs1060502639
ensemblrs1060502639
gopubmedrs1060502639
geneviewrs1060502639
scholarrs1060502639
googlers1060502639
pharmgkbrs1060502639
gwascentralrs1060502639
openSNPrs1060502639
23andMers1060502639
23andMe allrs1060502639
SNPshotrs1060502639
SNPdbers1060502639
MSV3drs1060502639
GWAS Ctlgrs1060502639
Max Magnitude0
ClinVar
Risk rs1060502639(T;T)
Alt rs1060502639(T;T)
Reference Rs1060502639(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32503174G>A
CLNSRC
CLNACC RCV000474172.1,