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rs587783591

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783591(A;T)
Make rs587783591(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111330997
GeneDCX
is asnp
is mentioned by
dbSNPrs587783591
ebirs587783591
HLIrs587783591
Exacrs587783591
Varsomers587783591
Maprs587783591
PheGenIrs587783591
hapmaprs587783591
1000 genomesrs587783591
hgdprs587783591
ensemblrs587783591
gopubmedrs587783591
geneviewrs587783591
scholarrs587783591
googlers587783591
pharmgkbrs587783591
gwascentralrs587783591
openSNPrs587783591
23andMers587783591
23andMe allrs587783591
SNP Nexus

SNPshotrs587783591
SNPdbers587783591
MSV3drs587783591
GWAS Ctlgrs587783591
Max Magnitude0
ClinVar
Risk rs587783591(T;T)
Alt rs587783591(T;T)
Reference rs587783591(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110574225T>A
CLNSRC
CLNACC RCV000145894.1,