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rs587783589

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783589(A;A)
Make rs587783589(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111331042
GeneDCX
is asnp
is mentioned by
dbSNPrs587783589
ebirs587783589
HLIrs587783589
Exacrs587783589
Varsomers587783589
Maprs587783589
PheGenIrs587783589
hapmaprs587783589
1000 genomesrs587783589
hgdprs587783589
ensemblrs587783589
gopubmedrs587783589
geneviewrs587783589
scholarrs587783589
googlers587783589
pharmgkbrs587783589
gwascentralrs587783589
openSNPrs587783589
23andMers587783589
23andMe allrs587783589
SNP Nexus

SNPshotrs587783589
SNPdbers587783589
MSV3drs587783589
GWAS Ctlgrs587783589
Max Magnitude0
ClinVar
Risk rs587783589(A;A)
Alt rs587783589(A;A)
Reference rs587783589(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110574270C>T
CLNSRC
CLNACC RCV000145892.1,