Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783542

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783542(A;T)
Make rs587783542(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410062
GeneDCX
is asnp
is mentioned by
dbSNPrs587783542
ClinGenrs587783542
ebirs587783542
HLIrs587783542
Exacrs587783542
Varsomers587783542
Maprs587783542
PheGenIrs587783542
hapmaprs587783542
1000 genomesrs587783542
hgdprs587783542
ensemblrs587783542
gopubmedrs587783542
geneviewrs587783542
scholarrs587783542
googlers587783542
pharmgkbrs587783542
gwascentralrs587783542
openSNPrs587783542
23andMers587783542
23andMe allrs587783542
SNP Nexus

SNPshotrs587783542
SNPdbers587783542
MSV3drs587783542
GWAS Ctlgrs587783542
Max Magnitude0
ClinVar
Risk rs587783542(T;T)
Alt rs587783542(T;T)
Reference Rs587783542(A;A)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653290T>A
CLNSRC
CLNACC RCV000145836.1,