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rs587783564

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783564(C;T)
Make rs587783564(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410344
GeneDCX
is asnp
is mentioned by
dbSNPrs587783564
ebirs587783564
HLIrs587783564
Exacrs587783564
Varsomers587783564
Maprs587783564
PheGenIrs587783564
hapmaprs587783564
1000 genomesrs587783564
hgdprs587783564
ensemblrs587783564
gopubmedrs587783564
geneviewrs587783564
scholarrs587783564
googlers587783564
pharmgkbrs587783564
gwascentralrs587783564
openSNPrs587783564
23andMers587783564
23andMe allrs587783564
SNP Nexus

SNPshotrs587783564
SNPdbers587783564
MSV3drs587783564
GWAS Ctlgrs587783564
Max Magnitude0
ClinVar
Risk rs587783564(T;T)
Alt rs587783564(T;T)
Reference rs587783564(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653572G>A
CLNSRC
CLNACC RCV000145861.1,