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

rs587783555

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587783555(-;-)
Make rs587783555(-;CA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401216
GeneDCX
is asnp
is mentioned by
dbSNPrs587783555
ebirs587783555
HLIrs587783555
Exacrs587783555
Varsomers587783555
Maprs587783555
PheGenIrs587783555
hapmaprs587783555
1000 genomesrs587783555
hgdprs587783555
ensemblrs587783555
gopubmedrs587783555
geneviewrs587783555
scholarrs587783555
googlers587783555
pharmgkbrs587783555
gwascentralrs587783555
openSNPrs587783555
23andMers587783555
23andMe allrs587783555
SNP Nexus

SNPshotrs587783555
SNPdbers587783555
MSV3drs587783555
GWAS Ctlgrs587783555
Max Magnitude0
ClinVar
Risk rs587783555(;)
Alt rs587783555(;)
Reference rs587783555(CA;CA)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644444_110644445delTG
CLNSRC
CLNACC RCV000145850.1,