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rs587783552

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783552(A;G)
Make rs587783552(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401282
GeneDCX
is asnp
is mentioned by
dbSNPrs587783552
ebirs587783552
HLIrs587783552
Exacrs587783552
Varsomers587783552
Maprs587783552
PheGenIrs587783552
hapmaprs587783552
1000 genomesrs587783552
hgdprs587783552
ensemblrs587783552
gopubmedrs587783552
geneviewrs587783552
scholarrs587783552
googlers587783552
pharmgkbrs587783552
gwascentralrs587783552
openSNPrs587783552
23andMers587783552
23andMe allrs587783552
SNP Nexus

SNPshotrs587783552
SNPdbers587783552
MSV3drs587783552
GWAS Ctlgrs587783552
Max Magnitude0
ClinVar
Risk rs587783552(G;G)
Alt rs587783552(G;G)
Reference rs587783552(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644510T>C
CLNSRC
CLNACC RCV000145846.1,