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rs587783522

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783522(C;T)
Make rs587783522(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410269
GeneDCX
is asnp
is mentioned by
dbSNPrs587783522
ebirs587783522
HLIrs587783522
Exacrs587783522
Varsomers587783522
Maprs587783522
PheGenIrs587783522
hapmaprs587783522
1000 genomesrs587783522
hgdprs587783522
ensemblrs587783522
gopubmedrs587783522
geneviewrs587783522
scholarrs587783522
googlers587783522
pharmgkbrs587783522
gwascentralrs587783522
openSNPrs587783522
23andMers587783522
23andMe allrs587783522
SNP Nexus

SNPshotrs587783522
SNPdbers587783522
MSV3drs587783522
GWAS Ctlgrs587783522
Max Magnitude0
ClinVar
Risk rs587783522(T;T)
Alt rs587783522(T;T)
Reference rs587783522(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653497G>A
CLNSRC
CLNACC RCV000145809.1,