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rs587783590

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783590(C;T)
Make rs587783590(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111331036
GeneDCX
is asnp
is mentioned by
dbSNPrs587783590
ebirs587783590
HLIrs587783590
Exacrs587783590
Varsomers587783590
Maprs587783590
PheGenIrs587783590
hapmaprs587783590
1000 genomesrs587783590
hgdprs587783590
ensemblrs587783590
gopubmedrs587783590
geneviewrs587783590
scholarrs587783590
googlers587783590
pharmgkbrs587783590
gwascentralrs587783590
openSNPrs587783590
23andMers587783590
23andMe allrs587783590
SNP Nexus

SNPshotrs587783590
SNPdbers587783590
MSV3drs587783590
GWAS Ctlgrs587783590
Max Magnitude0
ClinVar
Risk rs587783590(T;T)
Alt rs587783590(T;T)
Reference rs587783590(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110574264G>A
CLNSRC
CLNACC RCV000145893.1,