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rs104894783

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894783(A;C)
Make rs104894783(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position111410260
GeneDCX
is asnp
is mentioned by
dbSNPrs104894783
ebirs104894783
HLIrs104894783
Exacrs104894783
Varsomers104894783
Maprs104894783
PheGenIrs104894783
hapmaprs104894783
1000 genomesrs104894783
hgdprs104894783
ensemblrs104894783
gopubmedrs104894783
geneviewrs104894783
scholarrs104894783
googlers104894783
pharmgkbrs104894783
gwascentralrs104894783
openSNPrs104894783
23andMers104894783
23andMe allrs104894783
SNP Nexus

SNPshotrs104894783
SNPdbers104894783
MSV3drs104894783
GWAS Ctlgrs104894783
Max Magnitude0
OMIM300121
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104894783(C;C)
Alt rs104894783(C;C)
Reference rs104894783(A;A)
Significance Pathogenic
Disease Lissencephaly Subcortical laminar heterotopia
Variation info
Gene DCX
CLNDBN Lissencephaly, X-linked Subcortical laminar heterotopia, X-linked
Reversed 1
HGVS NC_000023.10:g.110653488T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012366.24, RCV000012367.24,