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rs587783574

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783574(C;C)
Make rs587783574(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401054
GeneDCX
is asnp
is mentioned by
dbSNPrs587783574
ebirs587783574
HLIrs587783574
Exacrs587783574
Varsomers587783574
Maprs587783574
PheGenIrs587783574
hapmaprs587783574
1000 genomesrs587783574
hgdprs587783574
ensemblrs587783574
gopubmedrs587783574
geneviewrs587783574
scholarrs587783574
googlers587783574
pharmgkbrs587783574
gwascentralrs587783574
openSNPrs587783574
23andMers587783574
23andMe allrs587783574
SNP Nexus

SNPshotrs587783574
SNPdbers587783574
MSV3drs587783574
GWAS Ctlgrs587783574
Max Magnitude0
ClinVar
Risk rs587783574(C;C)
Alt rs587783574(C;C)
Reference rs587783574(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644282A>G
CLNSRC
CLNACC RCV000145877.1,