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rs587783089

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783089(C;T)
Make rs587783089(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18588099
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783089
ebirs587783089
HLIrs587783089
Exacrs587783089
Varsomers587783089
Maprs587783089
PheGenIrs587783089
hapmaprs587783089
1000 genomesrs587783089
hgdprs587783089
ensemblrs587783089
gopubmedrs587783089
geneviewrs587783089
scholarrs587783089
googlers587783089
pharmgkbrs587783089
gwascentralrs587783089
openSNPrs587783089
23andMers587783089
23andMe allrs587783089
SNP Nexus

SNPshotrs587783089
SNPdbers587783089
MSV3drs587783089
GWAS Ctlgrs587783089
Max Magnitude0
ClinVar
Risk rs587783089(T;T)
Alt rs587783089(T;T)
Reference rs587783089(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18606219C>T
CLNSRC
CLNACC RCV000144751.1,