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rs587783533

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783533(C;T)
Make rs587783533(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410181
GeneDCX
is asnp
is mentioned by
dbSNPrs587783533
ebirs587783533
HLIrs587783533
Exacrs587783533
Varsomers587783533
Maprs587783533
PheGenIrs587783533
hapmaprs587783533
1000 genomesrs587783533
hgdprs587783533
ensemblrs587783533
gopubmedrs587783533
geneviewrs587783533
scholarrs587783533
googlers587783533
pharmgkbrs587783533
gwascentralrs587783533
openSNPrs587783533
23andMers587783533
23andMe allrs587783533
SNP Nexus

SNPshotrs587783533
SNPdbers587783533
MSV3drs587783533
GWAS Ctlgrs587783533
Max Magnitude0
ClinVar
Risk rs587783533(T;T)
Alt rs587783533(T;T)
Reference rs587783533(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653409G>A
CLNSRC
CLNACC RCV000145821.1,