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rs1057518284

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518284(-;AG)
Make rs1057518284(AG;AG)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32463504
GeneDMD
is asnp
is mentioned by
dbSNPrs1057518284
dbSNP (old)rs1057518284
ClinGenrs1057518284
ebirs1057518284
HLIrs1057518284
Exacrs1057518284
Gnomadrs1057518284
Varsomers1057518284
Maprs1057518284
PheGenIrs1057518284
Biobankrs1057518284
1000 genomesrs1057518284
hgdprs1057518284
ensemblrs1057518284
gopubmedrs1057518284
geneviewrs1057518284
scholarrs1057518284
googlers1057518284
pharmgkbrs1057518284
gwascentralrs1057518284
openSNPrs1057518284
23andMers1057518284
23andMe allrs1057518284
SNPshotrs1057518284
SNPdbers1057518284
MSV3drs1057518284
GWAS Ctlgrs1057518284
Max Magnitude0
ClinVar
Risk rs1057518284(AG;AG)
Alt rs1057518284(AG;AG)
Reference Rs1057518284(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32481622_32481623dupCT
CLNSRC
CLNACC RCV000412908.1,