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rs1060502629

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502629(A;A)
Make rs1060502629(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32573796
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502629
dbSNP (old)rs1060502629
ClinGenrs1060502629
ebirs1060502629
HLIrs1060502629
Exacrs1060502629
Gnomadrs1060502629
Varsomers1060502629
LitVarrs1060502629
Maprs1060502629
PheGenIrs1060502629
Biobankrs1060502629
1000 genomesrs1060502629
hgdprs1060502629
ensemblrs1060502629
gopubmedrs1060502629
geneviewrs1060502629
scholarrs1060502629
googlers1060502629
pharmgkbrs1060502629
gwascentralrs1060502629
openSNPrs1060502629
23andMers1060502629
23andMe allrs1060502629
SNPshotrs1060502629
SNPdbers1060502629
MSV3drs1060502629
GWAS Ctlgrs1060502629
Max Magnitude0
ClinVar
Risk rs1060502629(A;A)
Alt rs1060502629(A;A)
Reference Rs1060502629(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32591913C>T
CLNSRC
CLNACC RCV000469346.1,