Rs104894779

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894779(A;A)
Make rs104894779(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position111410215
GeneDCX
is asnp
is mentioned by
dbSNPrs104894779
PheGenIrs104894779
nextbiors104894779
hapmaprs104894779
1000 genomesrs104894779
hgdprs104894779
ensemblrs104894779
gopubmedrs104894779
geneviewrs104894779
scholarrs104894779
googlers104894779
pharmgkbrs104894779
gwascentralrs104894779
openSNPrs104894779
23andMers104894779
23andMe allrs104894779
SNP Nexus

SNPshotrs104894779
SNPdbers104894779
MSV3drs104894779
Max Magnitude0
OMIM300121
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894779(A;A)
Alt rs104894779(A;A)
Reference rs104894779(G;G)
Significance Pathogenic
Disease X-linked lissencephaly Subcortical laminar heterotopia
Variation info
Gene DCX
CLNDBN X-linked lissencephaly Subcortical laminar heterotopia, X-linked
Reversed 1
HGVS NC_000023.10:g.110653443C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012355.15, RCV000012356.23,