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

rs281865365

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865365(C;T)
Make rs281865365(T;T)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position18642042
GeneCDKL5, RS1
is asnp
is mentioned by
dbSNPrs281865365
dbSNP (classic)rs281865365
ClinGenrs281865365
ebirs281865365
HLIrs281865365
Exacrs281865365
Gnomadrs281865365
Varsomers281865365
LitVarrs281865365
Maprs281865365
PheGenIrs281865365
Biobankrs281865365
1000 genomesrs281865365
hgdprs281865365
ensemblrs281865365
geneviewrs281865365
scholarrs281865365
googlers281865365
pharmgkbrs281865365
gwascentralrs281865365
openSNPrs281865365
23andMers281865365
SNPshotrs281865365
SNPdbers281865365
MSV3drs281865365
GWAS Ctlgrs281865365
Max Magnitude0
ClinVar
Risk rs281865365(T;T)
Alt rs281865365(T;T)
Reference Rs281865365(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5 RS1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.18660162G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000085351.2,