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rs122457137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs122457137(G;T)
Make rs122457137(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position111410223
GeneDCX
is asnp
is mentioned by
dbSNPrs122457137
ebirs122457137
HLIrs122457137
Exacrs122457137
Varsomers122457137
Maprs122457137
PheGenIrs122457137
hapmaprs122457137
1000 genomesrs122457137
hgdprs122457137
ensemblrs122457137
gopubmedrs122457137
geneviewrs122457137
scholarrs122457137
googlers122457137
pharmgkbrs122457137
gwascentralrs122457137
openSNPrs122457137
23andMers122457137
23andMe allrs122457137
SNP Nexus

SNPshotrs122457137
SNPdbers122457137
MSV3drs122457137
GWAS Ctlgrs122457137
Max Magnitude0
OMIM300121
Desc
Variant0005
Relatedalso
ClinVar
Risk rs122457137(A,T;A,T)
Alt rs122457137(A,T;A,T)
Reference rs122457137(G;G)
Significance Pathogenic
Disease Lissencephaly Subcortical laminar heterotopia Heterotopia
Variation info
Gene DCX
CLNDBN Lissencephaly, X-linked Subcortical laminar heterotopia, X-linked Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653451C>A; NC_000023.10:g.110653451C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012362.22, RCV000012363.14, RCV000145814.1,