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rs587783524

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587783524(-;-)
Make rs587783524(-;AAAG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410245
GeneDCX
is asnp
is mentioned by
dbSNPrs587783524
ClinGenrs587783524
ebirs587783524
HLIrs587783524
Exacrs587783524
Varsomers587783524
Maprs587783524
PheGenIrs587783524
hapmaprs587783524
1000 genomesrs587783524
hgdprs587783524
ensemblrs587783524
gopubmedrs587783524
geneviewrs587783524
scholarrs587783524
googlers587783524
pharmgkbrs587783524
gwascentralrs587783524
openSNPrs587783524
23andMers587783524
23andMe allrs587783524
SNP Nexus

SNPshotrs587783524
SNPdbers587783524
MSV3drs587783524
GWAS Ctlgrs587783524
Max Magnitude0
ClinVar
Risk rs587783524(-;-)
Alt rs587783524(-;-)
Reference Rs587783524(AAAG;AAAG)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653473_110653476delCTTT
CLNSRC
CLNACC RCV000145811.1,