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rs587783557

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783557(A;G)
Make rs587783557(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401175
GeneDCX
is asnp
is mentioned by
dbSNPrs587783557
ebirs587783557
HLIrs587783557
Exacrs587783557
Varsomers587783557
Maprs587783557
PheGenIrs587783557
hapmaprs587783557
1000 genomesrs587783557
hgdprs587783557
ensemblrs587783557
gopubmedrs587783557
geneviewrs587783557
scholarrs587783557
googlers587783557
pharmgkbrs587783557
gwascentralrs587783557
openSNPrs587783557
23andMers587783557
23andMe allrs587783557
SNP Nexus

SNPshotrs587783557
SNPdbers587783557
MSV3drs587783557
GWAS Ctlgrs587783557
Max Magnitude0
ClinVar
Risk rs587783557(G;G)
Alt rs587783557(G;G)
Reference rs587783557(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644403T>C
CLNSRC
CLNACC RCV000145852.1,