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

rs587783544

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783544(A;A)
Make rs587783544(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410035
GeneDCX
is asnp
is mentioned by
dbSNPrs587783544
ebirs587783544
HLIrs587783544
Exacrs587783544
Varsomers587783544
Maprs587783544
PheGenIrs587783544
hapmaprs587783544
1000 genomesrs587783544
hgdprs587783544
ensemblrs587783544
gopubmedrs587783544
geneviewrs587783544
scholarrs587783544
googlers587783544
pharmgkbrs587783544
gwascentralrs587783544
openSNPrs587783544
23andMers587783544
23andMe allrs587783544
SNP Nexus

SNPshotrs587783544
SNPdbers587783544
MSV3drs587783544
GWAS Ctlgrs587783544
Max Magnitude0
ClinVar
Risk rs587783544(A;A)
Alt rs587783544(A;A)
Reference rs587783544(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653263C>T
CLNSRC
CLNACC RCV000145838.1,