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rs199469697

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs199469697(-;-)
Make rs199469697(-;C)
Make rs199469697(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position18642099
GeneCDKL5, RS1
is asnp
is mentioned by
dbSNPrs199469697
ebirs199469697
HLIrs199469697
Exacrs199469697
Varsomers199469697
Maprs199469697
PheGenIrs199469697
hapmaprs199469697
1000 genomesrs199469697
hgdprs199469697
ensemblrs199469697
gopubmedrs199469697
geneviewrs199469697
scholarrs199469697
googlers199469697
pharmgkbrs199469697
gwascentralrs199469697
openSNPrs199469697
23andMers199469697
23andMe allrs199469697
SNP Nexus

SNPshotrs199469697
SNPdbers199469697
MSV3drs199469697
GWAS Ctlgrs199469697
Max Magnitude0
ClinVar
Risk rs199469697(C;C)
Alt rs199469697(C;C)
Reference rs199469697(;)
Significance Untested
Disease not provided
Variation info
Gene CDKL5 RS1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.18660220dupG
CLNSRC ClinVar Retina International
CLNACC RCV000085336.1,