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

rs587783531

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783531(A;A)
Make rs587783531(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410204
GeneDCX
is asnp
is mentioned by
dbSNPrs587783531
ebirs587783531
HLIrs587783531
Exacrs587783531
Varsomers587783531
Maprs587783531
PheGenIrs587783531
hapmaprs587783531
1000 genomesrs587783531
hgdprs587783531
ensemblrs587783531
gopubmedrs587783531
geneviewrs587783531
scholarrs587783531
googlers587783531
pharmgkbrs587783531
gwascentralrs587783531
openSNPrs587783531
23andMers587783531
23andMe allrs587783531
SNP Nexus

SNPshotrs587783531
SNPdbers587783531
MSV3drs587783531
GWAS Ctlgrs587783531
Max Magnitude0
ClinVar
Risk rs587783531(A;A)
Alt rs587783531(A;A)
Reference rs587783531(C;C)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653432G>T
CLNSRC
CLNACC RCV000145819.1,