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rs587783569

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783569(C;C)
Make rs587783569(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401099
GeneDCX
is asnp
is mentioned by
dbSNPrs587783569
ebirs587783569
HLIrs587783569
Exacrs587783569
Varsomers587783569
Maprs587783569
PheGenIrs587783569
hapmaprs587783569
1000 genomesrs587783569
hgdprs587783569
ensemblrs587783569
gopubmedrs587783569
geneviewrs587783569
scholarrs587783569
googlers587783569
pharmgkbrs587783569
gwascentralrs587783569
openSNPrs587783569
23andMers587783569
23andMe allrs587783569
SNP Nexus

SNPshotrs587783569
SNPdbers587783569
MSV3drs587783569
GWAS Ctlgrs587783569
Max Magnitude0
ClinVar
Risk rs587783569(C;C)
Alt rs587783569(C;C)
Reference rs587783569(T;T)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644327A>G
CLNSRC
CLNACC RCV000145871.1,