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rs587783088

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783088(C;G)
Make rs587783088(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18588025
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783088
ebirs587783088
HLIrs587783088
Exacrs587783088
Varsomers587783088
Maprs587783088
PheGenIrs587783088
hapmaprs587783088
1000 genomesrs587783088
hgdprs587783088
ensemblrs587783088
gopubmedrs587783088
geneviewrs587783088
scholarrs587783088
googlers587783088
pharmgkbrs587783088
gwascentralrs587783088
openSNPrs587783088
23andMers587783088
23andMe allrs587783088
SNP Nexus

SNPshotrs587783088
SNPdbers587783088
MSV3drs587783088
GWAS Ctlgrs587783088
Max Magnitude0
ClinVar
Risk rs587783088(G;G)
Alt rs587783088(G;G)
Reference rs587783088(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18606145C>G
CLNSRC
CLNACC RCV000144750.2,