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rs199469701

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs199469701(-;-)
Make rs199469701(-;ATC)
Make rs199469701(ATC;ATC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position18642093
GeneCDKL5, RS1
is asnp
is mentioned by
dbSNPrs199469701
ebirs199469701
HLIrs199469701
Exacrs199469701
Varsomers199469701
Maprs199469701
PheGenIrs199469701
hapmaprs199469701
1000 genomesrs199469701
hgdprs199469701
ensemblrs199469701
gopubmedrs199469701
geneviewrs199469701
scholarrs199469701
googlers199469701
pharmgkbrs199469701
gwascentralrs199469701
openSNPrs199469701
23andMers199469701
23andMe allrs199469701
SNP Nexus

SNPshotrs199469701
SNPdbers199469701
MSV3drs199469701
GWAS Ctlgrs199469701
Max Magnitude0
ClinVar
Risk rs199469701(ATC;ATC)
Alt rs199469701(ATC;ATC)
Reference rs199469701(;)
Significance Untested
Disease not provided
Variation info
Gene CDKL5 RS1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.18660214_18660216dupGAT
CLNSRC ClinVar
CLNACC RCV000058881.1,