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rs587783583

From SNPedia

Orientationminus
Geno Mag Summary
(ATG;ATG) 0 common in clinvar
Make rs587783583(-;-)
Make rs587783583(-;ATG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333117
GeneDCX
is asnp
is mentioned by
dbSNPrs587783583
ebirs587783583
HLIrs587783583
Exacrs587783583
Varsomers587783583
Maprs587783583
PheGenIrs587783583
hapmaprs587783583
1000 genomesrs587783583
hgdprs587783583
ensemblrs587783583
gopubmedrs587783583
geneviewrs587783583
scholarrs587783583
googlers587783583
pharmgkbrs587783583
gwascentralrs587783583
openSNPrs587783583
23andMers587783583
23andMe allrs587783583
SNP Nexus

SNPshotrs587783583
SNPdbers587783583
MSV3drs587783583
GWAS Ctlgrs587783583
Max Magnitude0
ClinVar
Risk rs587783583(;)
Alt rs587783583(;)
Reference rs587783583(ATG;ATG)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110576345_110576347delCAT
CLNSRC
CLNACC RCV000145886.1,