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rs587783526

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783526(G;G)
Make rs587783526(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410229
GeneDCX
is asnp
is mentioned by
dbSNPrs587783526
ebirs587783526
HLIrs587783526
Exacrs587783526
Varsomers587783526
Maprs587783526
PheGenIrs587783526
hapmaprs587783526
1000 genomesrs587783526
hgdprs587783526
ensemblrs587783526
gopubmedrs587783526
geneviewrs587783526
scholarrs587783526
googlers587783526
pharmgkbrs587783526
gwascentralrs587783526
openSNPrs587783526
23andMers587783526
23andMe allrs587783526
SNP Nexus

SNPshotrs587783526
SNPdbers587783526
MSV3drs587783526
GWAS Ctlgrs587783526
Max Magnitude0
ClinVar
Risk rs587783526(G;G)
Alt rs587783526(G;G)
Reference rs587783526(T;T)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653457A>C
CLNSRC
CLNACC RCV000145813.1,