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rs587783079

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783079(A;A)
Make rs587783079(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18581888
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783079
ebirs587783079
HLIrs587783079
Exacrs587783079
Varsomers587783079
Maprs587783079
PheGenIrs587783079
hapmaprs587783079
1000 genomesrs587783079
hgdprs587783079
ensemblrs587783079
gopubmedrs587783079
geneviewrs587783079
scholarrs587783079
googlers587783079
pharmgkbrs587783079
gwascentralrs587783079
openSNPrs587783079
23andMers587783079
23andMe allrs587783079
SNP Nexus

SNPshotrs587783079
SNPdbers587783079
MSV3drs587783079
GWAS Ctlgrs587783079
Max Magnitude0
ClinVar
Risk rs587783079(A;A)
Alt rs587783079(A;A)
Reference rs587783079(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18600008C>A
CLNSRC
CLNACC RCV000144741.1,