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rs1060502620

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502620(-;-)
Make rs1060502620(-;A)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31932180
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502620
dbSNP (old)rs1060502620
ClinGenrs1060502620
ebirs1060502620
HLIrs1060502620
Exacrs1060502620
Gnomadrs1060502620
Varsomers1060502620
Maprs1060502620
PheGenIrs1060502620
Biobankrs1060502620
1000 genomesrs1060502620
hgdprs1060502620
ensemblrs1060502620
gopubmedrs1060502620
geneviewrs1060502620
scholarrs1060502620
googlers1060502620
pharmgkbrs1060502620
gwascentralrs1060502620
openSNPrs1060502620
23andMers1060502620
23andMe allrs1060502620
SNPshotrs1060502620
SNPdbers1060502620
MSV3drs1060502620
GWAS Ctlgrs1060502620
Max Magnitude0
ClinVar
Risk rs1060502620(-;-)
Alt rs1060502620(-;-)
Reference Rs1060502620(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31950297delT
CLNSRC
CLNACC RCV000470659.1,