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rs587783592

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783592(C;T)
Make rs587783592(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111330943
GeneDCX
is asnp
is mentioned by
dbSNPrs587783592
ebirs587783592
HLIrs587783592
Exacrs587783592
Varsomers587783592
Maprs587783592
PheGenIrs587783592
hapmaprs587783592
1000 genomesrs587783592
hgdprs587783592
ensemblrs587783592
gopubmedrs587783592
geneviewrs587783592
scholarrs587783592
googlers587783592
pharmgkbrs587783592
gwascentralrs587783592
openSNPrs587783592
23andMers587783592
23andMe allrs587783592
SNP Nexus

SNPshotrs587783592
SNPdbers587783592
MSV3drs587783592
GWAS Ctlgrs587783592
Max Magnitude0
ClinVar
Risk rs587783592(T;T)
Alt rs587783592(T;T)
Reference rs587783592(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110574171G>A
CLNSRC
CLNACC RCV000145895.1,