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rs587783546

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783546(A;A)
Make rs587783546(A;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401318
GeneDCX
is asnp
is mentioned by
dbSNPrs587783546
ebirs587783546
HLIrs587783546
Exacrs587783546
Varsomers587783546
Maprs587783546
PheGenIrs587783546
hapmaprs587783546
1000 genomesrs587783546
hgdprs587783546
ensemblrs587783546
gopubmedrs587783546
geneviewrs587783546
scholarrs587783546
googlers587783546
pharmgkbrs587783546
gwascentralrs587783546
openSNPrs587783546
23andMers587783546
23andMe allrs587783546
SNP Nexus

SNPshotrs587783546
SNPdbers587783546
MSV3drs587783546
GWAS Ctlgrs587783546
Max Magnitude0
ClinVar
Risk rs587783546(A;A)
Alt rs587783546(A;A)
Reference rs587783546(T;T)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644546A>T
CLNSRC
CLNACC RCV000145840.1,