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rs1064793742

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position31147421
GeneDMD
is asnp
is mentioned by
dbSNPrs1064793742
dbSNP (old)rs1064793742
ClinGenrs1064793742
ebirs1064793742
HLIrs1064793742
Exacrs1064793742
Gnomadrs1064793742
Varsomers1064793742
LitVarrs1064793742
Maprs1064793742
PheGenIrs1064793742
Biobankrs1064793742
1000 genomesrs1064793742
hgdprs1064793742
ensemblrs1064793742
gopubmedrs1064793742
geneviewrs1064793742
scholarrs1064793742
googlers1064793742
pharmgkbrs1064793742
gwascentralrs1064793742
openSNPrs1064793742
23andMers1064793742
23andMe allrs1064793742
SNPshotrs1064793742
SNPdbers1064793742
MSV3drs1064793742
GWAS Ctlgrs1064793742
Max Magnitude0
ClinVar
Risk rs1064793742(T;T)
Alt rs1064793742(T;T)
Reference Rs1064793742(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.31165538G>A
CLNSRC
CLNACC RCV000480741.1,