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rs587783078

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783078(G;G)
Make rs587783078(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18579921
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783078
dbSNP (classic)rs587783078
ClinGenrs587783078
ebirs587783078
HLIrs587783078
Exacrs587783078
Gnomadrs587783078
Varsomers587783078
LitVarrs587783078
Maprs587783078
PheGenIrs587783078
Biobankrs587783078
1000 genomesrs587783078
hgdprs587783078
ensemblrs587783078
geneviewrs587783078
scholarrs587783078
googlers587783078
pharmgkbrs587783078
gwascentralrs587783078
openSNPrs587783078
23andMers587783078
SNPshotrs587783078
SNPdbers587783078
MSV3drs587783078
GWAS Ctlgrs587783078
Max Magnitude0
ClinVar
Risk rs587783078(G;G)
Alt rs587783078(G;G)
Reference Rs587783078(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18598041T>G
CLNSRC
CLNACC RCV000144740.2,