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rs587783558

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783558(C;G)
Make rs587783558(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401163
GeneDCX
is asnp
is mentioned by
dbSNPrs587783558
ebirs587783558
HLIrs587783558
Exacrs587783558
Varsomers587783558
Maprs587783558
PheGenIrs587783558
hapmaprs587783558
1000 genomesrs587783558
hgdprs587783558
ensemblrs587783558
gopubmedrs587783558
geneviewrs587783558
scholarrs587783558
googlers587783558
pharmgkbrs587783558
gwascentralrs587783558
openSNPrs587783558
23andMers587783558
23andMe allrs587783558
SNP Nexus

SNPshotrs587783558
SNPdbers587783558
MSV3drs587783558
GWAS Ctlgrs587783558
Max Magnitude0
ClinVar
Risk rs587783558(G,T;G,T)
Alt rs587783558(G,T;G,T)
Reference rs587783558(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644391G>A; NC_000023.10:g.110644391G>C
CLNSRC
CLNACC RCV000145854.1, RCV000145853.1,