Rs104894781

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894781(C;C)
Make rs104894781(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position111401322
GeneDCX
is asnp
is mentioned by
dbSNPrs104894781
PheGenIrs104894781
nextbiors104894781
hapmaprs104894781
1000 genomesrs104894781
hgdprs104894781
ensemblrs104894781
gopubmedrs104894781
geneviewrs104894781
scholarrs104894781
googlers104894781
pharmgkbrs104894781
gwascentralrs104894781
openSNPrs104894781
23andMers104894781
23andMe allrs104894781
SNP Nexus

SNPshotrs104894781
SNPdbers104894781
MSV3drs104894781
Max Magnitude0
OMIM300121
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894781(C;C)
Alt rs104894781(C;C)
Reference rs104894781(T;T)
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.110644550A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012359.13, RCV000012360.13,