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rs587783576

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783576(-;-)
Make rs587783576(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401029
GeneDCX
is asnp
is mentioned by
dbSNPrs587783576
ebirs587783576
HLIrs587783576
Exacrs587783576
Varsomers587783576
Maprs587783576
PheGenIrs587783576
hapmaprs587783576
1000 genomesrs587783576
hgdprs587783576
ensemblrs587783576
gopubmedrs587783576
geneviewrs587783576
scholarrs587783576
googlers587783576
pharmgkbrs587783576
gwascentralrs587783576
openSNPrs587783576
23andMers587783576
23andMe allrs587783576
SNP Nexus

SNPshotrs587783576
SNPdbers587783576
MSV3drs587783576
GWAS Ctlgrs587783576
Max Magnitude0
ClinVar
Risk rs587783576(;)
Alt rs587783576(;)
Reference rs587783576(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644257delG
CLNSRC
CLNACC RCV000145879.1,