Rs104894779

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Orientationminus
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
GeneDCX
ChromosomeX
Orientationminus
Position110653443
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894779(A;A)
Make rs104894779(A;G)
OMIM300121
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894779(A;A)
Alt rs104894779(A;A)
Reference rs104894779(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.110653443C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012355.15, RCV000012356.23