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rs1060502630

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1060502630(-;AA)
Make rs1060502630(AA;AA)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31169589
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502630
dbSNP (classic)rs1060502630
ClinGenrs1060502630
ebirs1060502630
HLIrs1060502630
Exacrs1060502630
Gnomadrs1060502630
Varsomers1060502630
LitVarrs1060502630
Maprs1060502630
PheGenIrs1060502630
Biobankrs1060502630
1000 genomesrs1060502630
hgdprs1060502630
ensemblrs1060502630
geneviewrs1060502630
scholarrs1060502630
googlers1060502630
pharmgkbrs1060502630
gwascentralrs1060502630
openSNPrs1060502630
23andMers1060502630
23andMe allrs1060502630
SNPshotrs1060502630
SNPdbers1060502630
MSV3drs1060502630
GWAS Ctlgrs1060502630
Max Magnitude0
ClinVar
Risk rs1060502630(AA;AA)
Alt rs1060502630(AA;AA)
Reference Rs1060502630(-;-)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31187706_31187707insTT
CLNSRC
CLNACC RCV000475711.1,