Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783554

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783554(C;T)
Make rs587783554(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401217
GeneDCX
is asnp
is mentioned by
dbSNPrs587783554
ebirs587783554
HLIrs587783554
Exacrs587783554
Varsomers587783554
Maprs587783554
PheGenIrs587783554
hapmaprs587783554
1000 genomesrs587783554
hgdprs587783554
ensemblrs587783554
gopubmedrs587783554
geneviewrs587783554
scholarrs587783554
googlers587783554
pharmgkbrs587783554
gwascentralrs587783554
openSNPrs587783554
23andMers587783554
23andMe allrs587783554
SNP Nexus

SNPshotrs587783554
SNPdbers587783554
MSV3drs587783554
GWAS Ctlgrs587783554
Max Magnitude0
ClinVar
Risk rs587783554(T;T)
Alt rs587783554(T;T)
Reference rs587783554(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644445G>A
CLNSRC
CLNACC RCV000145849.1,