Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060502637

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502637(G;T)
Make rs1060502637(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32411914
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502637
dbSNP (old)rs1060502637
ClinGenrs1060502637
ebirs1060502637
HLIrs1060502637
Exacrs1060502637
Gnomadrs1060502637
Varsomers1060502637
Maprs1060502637
PheGenIrs1060502637
Biobankrs1060502637
1000 genomesrs1060502637
hgdprs1060502637
ensemblrs1060502637
gopubmedrs1060502637
geneviewrs1060502637
scholarrs1060502637
googlers1060502637
pharmgkbrs1060502637
gwascentralrs1060502637
openSNPrs1060502637
23andMers1060502637
23andMe allrs1060502637
SNPshotrs1060502637
SNPdbers1060502637
MSV3drs1060502637
GWAS Ctlgrs1060502637
Max Magnitude0
ClinVar
Risk rs1060502637(T;T)
Alt rs1060502637(T;T)
Reference Rs1060502637(G;G)
Significance Probable-Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32430031C>A
CLNSRC
CLNACC RCV000465065.1,