Rs104894784

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894784(A;A)
Make rs104894784(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position111410166
GeneDCX
is asnp
is mentioned by
dbSNPrs104894784
Exacrs104894784
PheGenIrs104894784
nextbiors104894784
hapmaprs104894784
1000 genomesrs104894784
hgdprs104894784
ensemblrs104894784
gopubmedrs104894784
geneviewrs104894784
scholarrs104894784
googlers104894784
pharmgkbrs104894784
gwascentralrs104894784
openSNPrs104894784
23andMers104894784
23andMe allrs104894784
SNP Nexus

SNPshotrs104894784
SNPdbers104894784
MSV3drs104894784
Max Magnitude0
OMIM300121
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104894784(A;A)
Alt rs104894784(A;A)
Reference rs104894784(G;G)
Significance Pathogenic
Disease Subcortical laminar heterotopia
Variation info
Gene DCX
CLNDBN Subcortical laminar heterotopia, X-linked
Reversed 1
HGVS NC_000023.10:g.110653394C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012371.23,