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

rs587783550

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783550(G;T)
Make rs587783550(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401286
GeneDCX
is asnp
is mentioned by
dbSNPrs587783550
ebirs587783550
HLIrs587783550
Exacrs587783550
Varsomers587783550
Maprs587783550
PheGenIrs587783550
hapmaprs587783550
1000 genomesrs587783550
hgdprs587783550
ensemblrs587783550
gopubmedrs587783550
geneviewrs587783550
scholarrs587783550
googlers587783550
pharmgkbrs587783550
gwascentralrs587783550
openSNPrs587783550
23andMers587783550
23andMe allrs587783550
SNP Nexus

SNPshotrs587783550
SNPdbers587783550
MSV3drs587783550
GWAS Ctlgrs587783550
Max Magnitude0
ClinVar
Risk rs587783550(T;T)
Alt rs587783550(T;T)
Reference rs587783550(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644514C>A
CLNSRC
CLNACC RCV000145844.1,