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rs1060502632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGGA;AGGA) 0 common in clinvar
Make rs1060502632(-;-)
Make rs1060502632(-;AGGA)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32365108
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502632
dbSNP (classic)rs1060502632
ClinGenrs1060502632
ebirs1060502632
HLIrs1060502632
Exacrs1060502632
Gnomadrs1060502632
Varsomers1060502632
LitVarrs1060502632
Maprs1060502632
PheGenIrs1060502632
Biobankrs1060502632
1000 genomesrs1060502632
hgdprs1060502632
ensemblrs1060502632
geneviewrs1060502632
scholarrs1060502632
googlers1060502632
pharmgkbrs1060502632
gwascentralrs1060502632
openSNPrs1060502632
23andMers1060502632
23andMe allrs1060502632
SNPshotrs1060502632
SNPdbers1060502632
MSV3drs1060502632
GWAS Ctlgrs1060502632
Max Magnitude0
ClinVar
Risk rs1060502632(-;-)
Alt rs1060502632(-;-)
Reference Rs1060502632(AGGA;AGGA)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32383225_32383228delTCCT
CLNSRC
CLNACC RCV000461657.1,