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rs587783586

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783586(A;T)
Make rs587783586(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333093
GeneDCX
is asnp
is mentioned by
dbSNPrs587783586
ebirs587783586
HLIrs587783586
Exacrs587783586
Varsomers587783586
Maprs587783586
PheGenIrs587783586
hapmaprs587783586
1000 genomesrs587783586
hgdprs587783586
ensemblrs587783586
gopubmedrs587783586
geneviewrs587783586
scholarrs587783586
googlers587783586
pharmgkbrs587783586
gwascentralrs587783586
openSNPrs587783586
23andMers587783586
23andMe allrs587783586
SNP Nexus

SNPshotrs587783586
SNPdbers587783586
MSV3drs587783586
GWAS Ctlgrs587783586
Max Magnitude0
ClinVar
Risk rs587783586(T;T)
Alt rs587783586(T;T)
Reference rs587783586(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110576321T>A
CLNSRC
CLNACC RCV000145889.1,