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rs587783082

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783082(C;T)
Make rs587783082(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18581908
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783082
ebirs587783082
HLIrs587783082
Exacrs587783082
Varsomers587783082
Maprs587783082
PheGenIrs587783082
hapmaprs587783082
1000 genomesrs587783082
hgdprs587783082
ensemblrs587783082
gopubmedrs587783082
geneviewrs587783082
scholarrs587783082
googlers587783082
pharmgkbrs587783082
gwascentralrs587783082
openSNPrs587783082
23andMers587783082
23andMe allrs587783082
SNP Nexus

SNPshotrs587783082
SNPdbers587783082
MSV3drs587783082
GWAS Ctlgrs587783082
Max Magnitude0
ClinVar
Risk rs587783082(T;T)
Alt rs587783082(T;T)
Reference rs587783082(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18600028C>T
CLNSRC
CLNACC RCV000144744.1,