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rs587783578

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783578(-;-)
Make rs587783578(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401025
GeneDCX
is asnp
is mentioned by
dbSNPrs587783578
ebirs587783578
HLIrs587783578
Exacrs587783578
Varsomers587783578
Maprs587783578
PheGenIrs587783578
hapmaprs587783578
1000 genomesrs587783578
hgdprs587783578
ensemblrs587783578
gopubmedrs587783578
geneviewrs587783578
scholarrs587783578
googlers587783578
pharmgkbrs587783578
gwascentralrs587783578
openSNPrs587783578
23andMers587783578
23andMe allrs587783578
SNP Nexus

SNPshotrs587783578
SNPdbers587783578
MSV3drs587783578
GWAS Ctlgrs587783578
Max Magnitude0
ClinVar
Risk rs587783578(;)
Alt rs587783578(;)
Reference rs587783578(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644253delC
CLNSRC
CLNACC RCV000145881.1,