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rs587783087

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783087(C;C)
Make rs587783087(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18588001
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783087
ebirs587783087
HLIrs587783087
Exacrs587783087
Varsomers587783087
Maprs587783087
PheGenIrs587783087
hapmaprs587783087
1000 genomesrs587783087
hgdprs587783087
ensemblrs587783087
gopubmedrs587783087
geneviewrs587783087
scholarrs587783087
googlers587783087
pharmgkbrs587783087
gwascentralrs587783087
openSNPrs587783087
23andMers587783087
23andMe allrs587783087
SNP Nexus

SNPshotrs587783087
SNPdbers587783087
MSV3drs587783087
GWAS Ctlgrs587783087
Max Magnitude0
ClinVar
Risk rs587783087(C;C)
Alt rs587783087(C;C)
Reference rs587783087(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18606121T>C
CLNSRC
CLNACC RCV000144749.1,