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rs587783540

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783540(A;A)
Make rs587783540(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410098
GeneDCX
is asnp
is mentioned by
dbSNPrs587783540
ebirs587783540
HLIrs587783540
Exacrs587783540
Varsomers587783540
Maprs587783540
PheGenIrs587783540
hapmaprs587783540
1000 genomesrs587783540
hgdprs587783540
ensemblrs587783540
gopubmedrs587783540
geneviewrs587783540
scholarrs587783540
googlers587783540
pharmgkbrs587783540
gwascentralrs587783540
openSNPrs587783540
23andMers587783540
23andMe allrs587783540
SNP Nexus

SNPshotrs587783540
SNPdbers587783540
MSV3drs587783540
GWAS Ctlgrs587783540
Max Magnitude0
ClinVar
Risk rs587783540(A;A)
Alt rs587783540(A;A)
Reference rs587783540(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653326C>T
CLNSRC
CLNACC RCV000145832.1,