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rs587783565

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783565(A;A)
Make rs587783565(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401124
GeneDCX
is asnp
is mentioned by
dbSNPrs587783565
ebirs587783565
HLIrs587783565
Exacrs587783565
Varsomers587783565
Maprs587783565
PheGenIrs587783565
hapmaprs587783565
1000 genomesrs587783565
hgdprs587783565
ensemblrs587783565
gopubmedrs587783565
geneviewrs587783565
scholarrs587783565
googlers587783565
pharmgkbrs587783565
gwascentralrs587783565
openSNPrs587783565
23andMers587783565
23andMe allrs587783565
SNP Nexus

SNPshotrs587783565
SNPdbers587783565
MSV3drs587783565
GWAS Ctlgrs587783565
Max Magnitude0
ClinVar
Risk rs587783565(A;A)
Alt rs587783565(A;A)
Reference rs587783565(C;C)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644352G>T
CLNSRC
CLNACC RCV000145862.1,