Have questions? Visit https://www.reddit.com/r/SNPedia

Rs104894780

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894780(C;T)
Make rs104894780(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position111401121
GeneDCX
is asnp
is mentioned by
dbSNPrs104894780
ebirs104894780
Exacrs104894780
PheGenIrs104894780
nextbiors104894780
hapmaprs104894780
1000 genomesrs104894780
hgdprs104894780
ensemblrs104894780
gopubmedrs104894780
geneviewrs104894780
scholarrs104894780
googlers104894780
pharmgkbrs104894780
gwascentralrs104894780
openSNPrs104894780
23andMers104894780
23andMe allrs104894780
SNP Nexus

SNPshotrs104894780
SNPdbers104894780
MSV3drs104894780
GWAS Ctlgrs104894780
Max Magnitude0
OMIM300121
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894780(T;T)
Alt rs104894780(T;T)
Reference rs104894780(C;C)
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_000023.11:g.111401121G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012357.15, RCV000012358.13, RCV000145864.1,