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rs587783566

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783566(C;G)
Make rs587783566(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401123
GeneDCX
is asnp
is mentioned by
dbSNPrs587783566
ebirs587783566
HLIrs587783566
Exacrs587783566
Varsomers587783566
Maprs587783566
PheGenIrs587783566
hapmaprs587783566
1000 genomesrs587783566
hgdprs587783566
ensemblrs587783566
gopubmedrs587783566
geneviewrs587783566
scholarrs587783566
googlers587783566
pharmgkbrs587783566
gwascentralrs587783566
openSNPrs587783566
23andMers587783566
23andMe allrs587783566
SNP Nexus

SNPshotrs587783566
SNPdbers587783566
MSV3drs587783566
GWAS Ctlgrs587783566
Max Magnitude0
ClinVar
Risk rs587783566(G;G)
Alt rs587783566(G;G)
Reference rs587783566(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644351G>C
CLNSRC
CLNACC RCV000145863.1,