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rs587783151

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783151(C;T)
Make rs587783151(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18604248
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783151
ebirs587783151
HLIrs587783151
Exacrs587783151
Varsomers587783151
Maprs587783151
PheGenIrs587783151
hapmaprs587783151
1000 genomesrs587783151
hgdprs587783151
ensemblrs587783151
gopubmedrs587783151
geneviewrs587783151
scholarrs587783151
googlers587783151
pharmgkbrs587783151
gwascentralrs587783151
openSNPrs587783151
23andMers587783151
23andMe allrs587783151
SNP Nexus

SNPshotrs587783151
SNPdbers587783151
MSV3drs587783151
GWAS Ctlgrs587783151
Max Magnitude0
ClinVar
Risk rs587783151(T;T)
Alt rs587783151(T;T)
Reference rs587783151(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18622368C>T
CLNSRC
CLNACC RCV000144827.1,