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rs587783581

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783581(A;C)
Make rs587783581(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401007
GeneDCX
is asnp
is mentioned by
dbSNPrs587783581
ebirs587783581
HLIrs587783581
Exacrs587783581
Varsomers587783581
Maprs587783581
PheGenIrs587783581
hapmaprs587783581
1000 genomesrs587783581
hgdprs587783581
ensemblrs587783581
gopubmedrs587783581
geneviewrs587783581
scholarrs587783581
googlers587783581
pharmgkbrs587783581
gwascentralrs587783581
openSNPrs587783581
23andMers587783581
23andMe allrs587783581
SNP Nexus

SNPshotrs587783581
SNPdbers587783581
MSV3drs587783581
GWAS Ctlgrs587783581
Max Magnitude0
ClinVar
Risk rs587783581(C;C)
Alt rs587783581(C;C)
Reference rs587783581(A;A)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644235T>G
CLNSRC
CLNACC RCV000145884.1,