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rs587783584

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783584(G;G)
Make rs587783584(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333113
GeneDCX
is asnp
is mentioned by
dbSNPrs587783584
ClinGenrs587783584
ebirs587783584
HLIrs587783584
Exacrs587783584
Varsomers587783584
Maprs587783584
PheGenIrs587783584
hapmaprs587783584
1000 genomesrs587783584
hgdprs587783584
ensemblrs587783584
gopubmedrs587783584
geneviewrs587783584
scholarrs587783584
googlers587783584
pharmgkbrs587783584
gwascentralrs587783584
openSNPrs587783584
23andMers587783584
23andMe allrs587783584
SNP Nexus

SNPshotrs587783584
SNPdbers587783584
MSV3drs587783584
GWAS Ctlgrs587783584
Max Magnitude0
ClinVar
Risk rs587783584(G;G)
Alt rs587783584(G;G)
Reference Rs587783584(T;T)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110576341A>C
CLNSRC
CLNACC RCV000145887.1,