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rs587783117

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587783117(-;-)
Make rs587783117(-;TT)
Make rs587783117(TT;TT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18604810
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783117
ebirs587783117
HLIrs587783117
Exacrs587783117
Varsomers587783117
Maprs587783117
PheGenIrs587783117
hapmaprs587783117
1000 genomesrs587783117
hgdprs587783117
ensemblrs587783117
gopubmedrs587783117
geneviewrs587783117
scholarrs587783117
googlers587783117
pharmgkbrs587783117
gwascentralrs587783117
openSNPrs587783117
23andMers587783117
23andMe allrs587783117
SNP Nexus

SNPshotrs587783117
SNPdbers587783117
MSV3drs587783117
GWAS Ctlgrs587783117
Max Magnitude0
ClinVar
Risk rs587783117(TT;TT)
Alt rs587783117(TT;TT)
Reference rs587783117(;)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18622929_18622930dupTT
CLNSRC
CLNACC RCV000144788.1,