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rs1060502625

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502625(-;-)
Make rs1060502625(-;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31147347
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502625
dbSNP (old)rs1060502625
ClinGenrs1060502625
ebirs1060502625
HLIrs1060502625
Exacrs1060502625
Gnomadrs1060502625
Varsomers1060502625
LitVarrs1060502625
Maprs1060502625
PheGenIrs1060502625
Biobankrs1060502625
1000 genomesrs1060502625
hgdprs1060502625
ensemblrs1060502625
gopubmedrs1060502625
geneviewrs1060502625
scholarrs1060502625
googlers1060502625
pharmgkbrs1060502625
gwascentralrs1060502625
openSNPrs1060502625
23andMers1060502625
23andMe allrs1060502625
SNPshotrs1060502625
SNPdbers1060502625
MSV3drs1060502625
GWAS Ctlgrs1060502625
Max Magnitude0
ClinVar
Risk rs1060502625(-;-)
Alt rs1060502625(-;-)
Reference Rs1060502625(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31165464delC
CLNSRC
CLNACC RCV000473878.1,