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rs1060502647

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs1060502647(-;-)
Make rs1060502647(-;AC)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32364635
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502647
dbSNP (old)rs1060502647
ClinGenrs1060502647
ebirs1060502647
HLIrs1060502647
Exacrs1060502647
Gnomadrs1060502647
Varsomers1060502647
Maprs1060502647
PheGenIrs1060502647
Biobankrs1060502647
1000 genomesrs1060502647
hgdprs1060502647
ensemblrs1060502647
gopubmedrs1060502647
geneviewrs1060502647
scholarrs1060502647
googlers1060502647
pharmgkbrs1060502647
gwascentralrs1060502647
openSNPrs1060502647
23andMers1060502647
23andMe allrs1060502647
SNPshotrs1060502647
SNPdbers1060502647
MSV3drs1060502647
GWAS Ctlgrs1060502647
Max Magnitude0
ClinVar
Risk rs1060502647(-;-)
Alt rs1060502647(-;-)
Reference Rs1060502647(AC;AC)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32382752_32382753delGT
CLNSRC
CLNACC RCV000473975.1,