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rs587783519

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783519(C;T)
Make rs587783519(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410284
GeneDCX
is asnp
is mentioned by
dbSNPrs587783519
ebirs587783519
HLIrs587783519
Exacrs587783519
Varsomers587783519
Maprs587783519
PheGenIrs587783519
hapmaprs587783519
1000 genomesrs587783519
hgdprs587783519
ensemblrs587783519
gopubmedrs587783519
geneviewrs587783519
scholarrs587783519
googlers587783519
pharmgkbrs587783519
gwascentralrs587783519
openSNPrs587783519
23andMers587783519
23andMe allrs587783519
SNP Nexus

SNPshotrs587783519
SNPdbers587783519
MSV3drs587783519
GWAS Ctlgrs587783519
Max Magnitude0
ClinVar
Risk rs587783519(T;T)
Alt rs587783519(T;T)
Reference rs587783519(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653512G>A
CLNSRC
CLNACC RCV000145806.1,