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rs587783559

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783559(G;T)
Make rs587783559(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401162
GeneDCX
is asnp
is mentioned by
dbSNPrs587783559
ebirs587783559
HLIrs587783559
Exacrs587783559
Varsomers587783559
Maprs587783559
PheGenIrs587783559
hapmaprs587783559
1000 genomesrs587783559
hgdprs587783559
ensemblrs587783559
gopubmedrs587783559
geneviewrs587783559
scholarrs587783559
googlers587783559
pharmgkbrs587783559
gwascentralrs587783559
openSNPrs587783559
23andMers587783559
23andMe allrs587783559
SNP Nexus

SNPshotrs587783559
SNPdbers587783559
MSV3drs587783559
GWAS Ctlgrs587783559
Max Magnitude0
ClinVar
Risk rs587783559(T;T)
Alt rs587783559(T;T)
Reference rs587783559(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644390C>A
CLNSRC
CLNACC RCV000145855.1,