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rs587783545

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783545(-;-)
Make rs587783545(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401328
GeneDCX
is asnp
is mentioned by
dbSNPrs587783545
ebirs587783545
HLIrs587783545
Exacrs587783545
Varsomers587783545
Maprs587783545
PheGenIrs587783545
hapmaprs587783545
1000 genomesrs587783545
hgdprs587783545
ensemblrs587783545
gopubmedrs587783545
geneviewrs587783545
scholarrs587783545
googlers587783545
pharmgkbrs587783545
gwascentralrs587783545
openSNPrs587783545
23andMers587783545
23andMe allrs587783545
SNP Nexus

SNPshotrs587783545
SNPdbers587783545
MSV3drs587783545
GWAS Ctlgrs587783545
Max Magnitude0
ClinVar
Risk rs587783545(;)
Alt rs587783545(;)
Reference rs587783545(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644556delC
CLNSRC
CLNACC RCV000145839.1,