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rs1057518692

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518692(-;-)
Make rs1057518692(-;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32343221
GeneDMD
is asnp
is mentioned by
dbSNPrs1057518692
dbSNP (old)rs1057518692
ClinGenrs1057518692
ebirs1057518692
HLIrs1057518692
Exacrs1057518692
Gnomadrs1057518692
Varsomers1057518692
LitVarrs1057518692
Maprs1057518692
PheGenIrs1057518692
Biobankrs1057518692
1000 genomesrs1057518692
hgdprs1057518692
ensemblrs1057518692
gopubmedrs1057518692
geneviewrs1057518692
scholarrs1057518692
googlers1057518692
pharmgkbrs1057518692
gwascentralrs1057518692
openSNPrs1057518692
23andMers1057518692
23andMe allrs1057518692
SNPshotrs1057518692
SNPdbers1057518692
MSV3drs1057518692
GWAS Ctlgrs1057518692
Max Magnitude0
ClinVar
Risk rs1057518692(-;-)
Alt rs1057518692(-;-)
Reference Rs1057518692(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32361338delC
CLNSRC
CLNACC RCV000415013.1,