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rs587783536

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783536(C;C)
Make rs587783536(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410127
GeneDCX
is asnp
is mentioned by
dbSNPrs587783536
ebirs587783536
HLIrs587783536
Exacrs587783536
Varsomers587783536
Maprs587783536
PheGenIrs587783536
hapmaprs587783536
1000 genomesrs587783536
hgdprs587783536
ensemblrs587783536
gopubmedrs587783536
geneviewrs587783536
scholarrs587783536
googlers587783536
pharmgkbrs587783536
gwascentralrs587783536
openSNPrs587783536
23andMers587783536
23andMe allrs587783536
SNP Nexus

SNPshotrs587783536
SNPdbers587783536
MSV3drs587783536
GWAS Ctlgrs587783536
Max Magnitude0
ClinVar
Risk rs587783536(C;C)
Alt rs587783536(C;C)
Reference rs587783536(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653355A>G
CLNSRC
CLNACC RCV000145827.1,