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rs1060502656

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502656(A;A)
Make rs1060502656(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32287702
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502656
dbSNP (old)rs1060502656
ClinGenrs1060502656
ebirs1060502656
HLIrs1060502656
Exacrs1060502656
Gnomadrs1060502656
Varsomers1060502656
Maprs1060502656
PheGenIrs1060502656
Biobankrs1060502656
1000 genomesrs1060502656
hgdprs1060502656
ensemblrs1060502656
gopubmedrs1060502656
geneviewrs1060502656
scholarrs1060502656
googlers1060502656
pharmgkbrs1060502656
gwascentralrs1060502656
openSNPrs1060502656
23andMers1060502656
23andMe allrs1060502656
SNPshotrs1060502656
SNPdbers1060502656
MSV3drs1060502656
GWAS Ctlgrs1060502656
Max Magnitude0
ClinVar
Risk rs1060502656(A;A)
Alt rs1060502656(A;A)
Reference Rs1060502656(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32305819C>T
CLNSRC
CLNACC RCV000469689.1,