Rs104894786

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894786
PheGenIrs104894786
nextbiors104894786
hapmaprs104894786
1000 genomesrs104894786
hgdprs104894786
ensemblrs104894786
gopubmedrs104894786
geneviewrs104894786
scholarrs104894786
googlers104894786
pharmgkbrs104894786
gwascentralrs104894786
openSNPrs104894786
23andMers104894786
23andMe allrs104894786
SNP Nexus

SNPshotrs104894786
SNPdbers104894786
MSV3drs104894786
GeneDCX
ChromosomeX
Orientationminus
Position111410188
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894786(G;T)
Make rs104894786(T;T)
OMIM300121
Desc
Variant0014
Relatedalso
ClinVar
Risk rs104894786(T;T)
Alt rs104894786(T;T)
Reference rs104894786(G;G)
Significance 5
Disease X-linked lissencephaly, Subcortical laminar heterotopia
ClinVar info
Gene DCX
CLNDBN X-linked lissencephaly, Subcortical laminar heterotopia, X-linked
Reversed 1
CLNHGVS NC_000023.10:g.110653416C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012375.13, RCV000012376.15