Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783080

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783080(A;G)
Make rs587783080(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18581889
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783080
ebirs587783080
HLIrs587783080
Exacrs587783080
Varsomers587783080
Maprs587783080
PheGenIrs587783080
hapmaprs587783080
1000 genomesrs587783080
hgdprs587783080
ensemblrs587783080
gopubmedrs587783080
geneviewrs587783080
scholarrs587783080
googlers587783080
pharmgkbrs587783080
gwascentralrs587783080
openSNPrs587783080
23andMers587783080
23andMe allrs587783080
SNP Nexus

SNPshotrs587783080
SNPdbers587783080
MSV3drs587783080
GWAS Ctlgrs587783080
Max Magnitude0
ClinVar
Risk rs587783080(G;G)
Alt rs587783080(G;G)
Reference rs587783080(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18600009A>G
CLNSRC
CLNACC RCV000144742.2,