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rs587783518

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783518(A;G)
Make rs587783518(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111301745
GeneDCX
is asnp
is mentioned by
dbSNPrs587783518
ebirs587783518
HLIrs587783518
Exacrs587783518
Varsomers587783518
Maprs587783518
PheGenIrs587783518
hapmaprs587783518
1000 genomesrs587783518
hgdprs587783518
ensemblrs587783518
gopubmedrs587783518
geneviewrs587783518
scholarrs587783518
googlers587783518
pharmgkbrs587783518
gwascentralrs587783518
openSNPrs587783518
23andMers587783518
23andMe allrs587783518
SNP Nexus

SNPshotrs587783518
SNPdbers587783518
MSV3drs587783518
GWAS Ctlgrs587783518
Max Magnitude0
ClinVar
Risk rs587783518(G;G)
Alt rs587783518(G;G)
Reference rs587783518(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110544973T>C
CLNSRC
CLNACC RCV000145805.1,