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rs587783575

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783575(-;-)
Make rs587783575(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401044
GeneDCX
is asnp
is mentioned by
dbSNPrs587783575
ebirs587783575
HLIrs587783575
Exacrs587783575
Varsomers587783575
Maprs587783575
PheGenIrs587783575
hapmaprs587783575
1000 genomesrs587783575
hgdprs587783575
ensemblrs587783575
gopubmedrs587783575
geneviewrs587783575
scholarrs587783575
googlers587783575
pharmgkbrs587783575
gwascentralrs587783575
openSNPrs587783575
23andMers587783575
23andMe allrs587783575
SNP Nexus

SNPshotrs587783575
SNPdbers587783575
MSV3drs587783575
GWAS Ctlgrs587783575
Max Magnitude0
ClinVar
Risk rs587783575(;)
Alt rs587783575(;)
Reference rs587783575(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644272delG
CLNSRC
CLNACC RCV000145878.1,