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rs587783525

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783525(C;C)
Make rs587783525(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410232
GeneDCX
is asnp
is mentioned by
dbSNPrs587783525
ebirs587783525
HLIrs587783525
Exacrs587783525
Varsomers587783525
Maprs587783525
PheGenIrs587783525
hapmaprs587783525
1000 genomesrs587783525
hgdprs587783525
ensemblrs587783525
gopubmedrs587783525
geneviewrs587783525
scholarrs587783525
googlers587783525
pharmgkbrs587783525
gwascentralrs587783525
openSNPrs587783525
23andMers587783525
23andMe allrs587783525
SNP Nexus

SNPshotrs587783525
SNPdbers587783525
MSV3drs587783525
GWAS Ctlgrs587783525
Max Magnitude0
ClinVar
Risk rs587783525(C;C)
Alt rs587783525(C;C)
Reference rs587783525(G;G)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653460C>G
CLNSRC
CLNACC RCV000145812.1,