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rs587783534

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783534(C;T)
Make rs587783534(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410173
GeneDCX
is asnp
is mentioned by
dbSNPrs587783534
ebirs587783534
HLIrs587783534
Exacrs587783534
Varsomers587783534
Maprs587783534
PheGenIrs587783534
hapmaprs587783534
1000 genomesrs587783534
hgdprs587783534
ensemblrs587783534
gopubmedrs587783534
geneviewrs587783534
scholarrs587783534
googlers587783534
pharmgkbrs587783534
gwascentralrs587783534
openSNPrs587783534
23andMers587783534
23andMe allrs587783534
SNP Nexus

SNPshotrs587783534
SNPdbers587783534
MSV3drs587783534
GWAS Ctlgrs587783534
Max Magnitude0
ClinVar
Risk rs587783534(T;T)
Alt rs587783534(T;T)
Reference rs587783534(C;C)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653401G>A
CLNSRC
CLNACC RCV000145822.1,