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rs587783551

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783551(C;C)
Make rs587783551(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401283
GeneDCX
is asnp
is mentioned by
dbSNPrs587783551
ebirs587783551
HLIrs587783551
Exacrs587783551
Varsomers587783551
Maprs587783551
PheGenIrs587783551
hapmaprs587783551
1000 genomesrs587783551
hgdprs587783551
ensemblrs587783551
gopubmedrs587783551
geneviewrs587783551
scholarrs587783551
googlers587783551
pharmgkbrs587783551
gwascentralrs587783551
openSNPrs587783551
23andMers587783551
23andMe allrs587783551
SNP Nexus

SNPshotrs587783551
SNPdbers587783551
MSV3drs587783551
GWAS Ctlgrs587783551
Max Magnitude0
ClinVar
Risk rs587783551(C;C)
Alt rs587783551(C;C)
Reference rs587783551(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644511A>G
CLNSRC
CLNACC RCV000145845.1,