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rs587783530

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783530(A;G)
Make rs587783530(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410208
GeneDCX
is asnp
is mentioned by
dbSNPrs587783530
ebirs587783530
HLIrs587783530
Exacrs587783530
Varsomers587783530
Maprs587783530
PheGenIrs587783530
hapmaprs587783530
1000 genomesrs587783530
hgdprs587783530
ensemblrs587783530
gopubmedrs587783530
geneviewrs587783530
scholarrs587783530
googlers587783530
pharmgkbrs587783530
gwascentralrs587783530
openSNPrs587783530
23andMers587783530
23andMe allrs587783530
SNP Nexus

SNPshotrs587783530
SNPdbers587783530
MSV3drs587783530
GWAS Ctlgrs587783530
Max Magnitude0
ClinVar
Risk rs587783530(G;G)
Alt rs587783530(G;G)
Reference rs587783530(A;A)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653436T>C
CLNSRC
CLNACC RCV000145818.1,