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rs587783588

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783588(C;T)
Make rs587783588(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333078
GeneDCX
is asnp
is mentioned by
dbSNPrs587783588
ebirs587783588
HLIrs587783588
Exacrs587783588
Varsomers587783588
Maprs587783588
PheGenIrs587783588
hapmaprs587783588
1000 genomesrs587783588
hgdprs587783588
ensemblrs587783588
gopubmedrs587783588
geneviewrs587783588
scholarrs587783588
googlers587783588
pharmgkbrs587783588
gwascentralrs587783588
openSNPrs587783588
23andMers587783588
23andMe allrs587783588
SNP Nexus

SNPshotrs587783588
SNPdbers587783588
MSV3drs587783588
GWAS Ctlgrs587783588
Max Magnitude0
ClinVar
Risk rs587783588(T;T)
Alt rs587783588(T;T)
Reference rs587783588(C;C)
Significance Pathogenic
Disease Heterotopia Lissencephaly
Variation info
Gene DCX
CLNDBN Heterotopia Lissencephaly, X-linked
Reversed 1
HGVS NC_000023.10:g.110576306G>A
CLNSRC
CLNACC RCV000145891.1, RCV000178405.1,