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rs587783570

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783570(A;G)
Make rs587783570(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401088
GeneDCX
is asnp
is mentioned by
dbSNPrs587783570
ebirs587783570
HLIrs587783570
Exacrs587783570
Varsomers587783570
Maprs587783570
PheGenIrs587783570
hapmaprs587783570
1000 genomesrs587783570
hgdprs587783570
ensemblrs587783570
gopubmedrs587783570
geneviewrs587783570
scholarrs587783570
googlers587783570
pharmgkbrs587783570
gwascentralrs587783570
openSNPrs587783570
23andMers587783570
23andMe allrs587783570
SNP Nexus

SNPshotrs587783570
SNPdbers587783570
MSV3drs587783570
GWAS Ctlgrs587783570
Max Magnitude0
ClinVar
Risk rs587783570(G;G)
Alt rs587783570(G;G)
Reference rs587783570(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644316T>C
CLNSRC
CLNACC RCV000145872.1,