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rs587783535

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783535(C;T)
Make rs587783535(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410167
GeneDCX
is asnp
is mentioned by
dbSNPrs587783535
ebirs587783535
HLIrs587783535
Exacrs587783535
Varsomers587783535
Maprs587783535
PheGenIrs587783535
hapmaprs587783535
1000 genomesrs587783535
hgdprs587783535
ensemblrs587783535
gopubmedrs587783535
geneviewrs587783535
scholarrs587783535
googlers587783535
pharmgkbrs587783535
gwascentralrs587783535
openSNPrs587783535
23andMers587783535
23andMe allrs587783535
SNP Nexus

SNPshotrs587783535
SNPdbers587783535
MSV3drs587783535
GWAS Ctlgrs587783535
Max Magnitude0
ClinVar
Risk rs587783535(T;T)
Alt rs587783535(T;T)
Reference rs587783535(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653395G>A
CLNSRC
CLNACC RCV000145823.1,