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rs587783582

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783582(A;A)
Make rs587783582(A;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333135
GeneDCX
is asnp
is mentioned by
dbSNPrs587783582
ebirs587783582
HLIrs587783582
Exacrs587783582
Varsomers587783582
Maprs587783582
PheGenIrs587783582
hapmaprs587783582
1000 genomesrs587783582
hgdprs587783582
ensemblrs587783582
gopubmedrs587783582
geneviewrs587783582
scholarrs587783582
googlers587783582
pharmgkbrs587783582
gwascentralrs587783582
openSNPrs587783582
23andMers587783582
23andMe allrs587783582
SNP Nexus

SNPshotrs587783582
SNPdbers587783582
MSV3drs587783582
GWAS Ctlgrs587783582
Max Magnitude0
ClinVar
Risk rs587783582(A;A)
Alt rs587783582(A;A)
Reference rs587783582(T;T)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110576363A>T
CLNSRC
CLNACC RCV000145885.1,