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rs587783560

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783560(A;G)
Make rs587783560(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401157
GeneDCX
is asnp
is mentioned by
dbSNPrs587783560
ebirs587783560
HLIrs587783560
Exacrs587783560
Varsomers587783560
Maprs587783560
PheGenIrs587783560
hapmaprs587783560
1000 genomesrs587783560
hgdprs587783560
ensemblrs587783560
gopubmedrs587783560
geneviewrs587783560
scholarrs587783560
googlers587783560
pharmgkbrs587783560
gwascentralrs587783560
openSNPrs587783560
23andMers587783560
23andMe allrs587783560
SNP Nexus

SNPshotrs587783560
SNPdbers587783560
MSV3drs587783560
GWAS Ctlgrs587783560
Max Magnitude0
ClinVar
Risk rs587783560(G;G)
Alt rs587783560(G;G)
Reference rs587783560(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644385T>C
CLNSRC
CLNACC RCV000145856.1,