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rs1060502652

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1060502652(-;-)
Make rs1060502652(-;GA)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position33020191
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502652
dbSNP (old)rs1060502652
ClinGenrs1060502652
ebirs1060502652
HLIrs1060502652
Exacrs1060502652
Gnomadrs1060502652
Varsomers1060502652
Maprs1060502652
PheGenIrs1060502652
Biobankrs1060502652
1000 genomesrs1060502652
hgdprs1060502652
ensemblrs1060502652
gopubmedrs1060502652
geneviewrs1060502652
scholarrs1060502652
googlers1060502652
pharmgkbrs1060502652
gwascentralrs1060502652
openSNPrs1060502652
23andMers1060502652
23andMe allrs1060502652
SNPshotrs1060502652
SNPdbers1060502652
MSV3drs1060502652
GWAS Ctlgrs1060502652
Max Magnitude0
ClinVar
Risk rs1060502652(-;-)
Alt rs1060502652(-;-)
Reference Rs1060502652(GA;GA)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.33038308_33038309delTC
CLNSRC
CLNACC RCV000468912.1,