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rs587783571

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783571(A;A)
Make rs587783571(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401084
GeneDCX
is asnp
is mentioned by
dbSNPrs587783571
ebirs587783571
HLIrs587783571
Exacrs587783571
Varsomers587783571
Maprs587783571
PheGenIrs587783571
hapmaprs587783571
1000 genomesrs587783571
hgdprs587783571
ensemblrs587783571
gopubmedrs587783571
geneviewrs587783571
scholarrs587783571
googlers587783571
pharmgkbrs587783571
gwascentralrs587783571
openSNPrs587783571
23andMers587783571
23andMe allrs587783571
SNP Nexus

SNPshotrs587783571
SNPdbers587783571
MSV3drs587783571
GWAS Ctlgrs587783571
Max Magnitude0
ClinVar
Risk rs587783571(A;A)
Alt rs587783571(A;A)
Reference rs587783571(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644312G>T
CLNSRC
CLNACC RCV000145874.1,