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rs587783562

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783562(C;T)
Make rs587783562(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401139
GeneDCX
is asnp
is mentioned by
dbSNPrs587783562
ebirs587783562
HLIrs587783562
Exacrs587783562
Varsomers587783562
Maprs587783562
PheGenIrs587783562
hapmaprs587783562
1000 genomesrs587783562
hgdprs587783562
ensemblrs587783562
gopubmedrs587783562
geneviewrs587783562
scholarrs587783562
googlers587783562
pharmgkbrs587783562
gwascentralrs587783562
openSNPrs587783562
23andMers587783562
23andMe allrs587783562
SNP Nexus

SNPshotrs587783562
SNPdbers587783562
MSV3drs587783562
GWAS Ctlgrs587783562
Max Magnitude0
ClinVar
Risk rs587783562(T;T)
Alt rs587783562(T;T)
Reference rs587783562(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644367G>A
CLNSRC
CLNACC RCV000145858.1,