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rs587783572

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783572(A;T)
Make rs587783572(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401081
GeneDCX
is asnp
is mentioned by
dbSNPrs587783572
ebirs587783572
HLIrs587783572
Exacrs587783572
Varsomers587783572
Maprs587783572
PheGenIrs587783572
hapmaprs587783572
1000 genomesrs587783572
hgdprs587783572
ensemblrs587783572
gopubmedrs587783572
geneviewrs587783572
scholarrs587783572
googlers587783572
pharmgkbrs587783572
gwascentralrs587783572
openSNPrs587783572
23andMers587783572
23andMe allrs587783572
SNP Nexus

SNPshotrs587783572
SNPdbers587783572
MSV3drs587783572
GWAS Ctlgrs587783572
Max Magnitude0
ClinVar
Risk rs587783572(T;T)
Alt rs587783572(T;T)
Reference rs587783572(A;A)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644309T>A
CLNSRC
CLNACC RCV000145875.1,