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rs199469698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199469698(C;C)
Make rs199469698(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position18644576
GeneCDKL5, RS1
is asnp
is mentioned by
dbSNPrs199469698
ebirs199469698
HLIrs199469698
Exacrs199469698
Varsomers199469698
Maprs199469698
PheGenIrs199469698
hapmaprs199469698
1000 genomesrs199469698
hgdprs199469698
ensemblrs199469698
gopubmedrs199469698
geneviewrs199469698
scholarrs199469698
googlers199469698
pharmgkbrs199469698
gwascentralrs199469698
openSNPrs199469698
23andMers199469698
23andMe allrs199469698
SNP Nexus

SNPshotrs199469698
SNPdbers199469698
MSV3drs199469698
GWAS Ctlgrs199469698
Max Magnitude0
ClinVar
Risk rs199469698(C;C)
Alt rs199469698(C;C)
Reference rs199469698(G;G)
Significance Untested
Disease not provided
Variation info
Gene CDKL5 RS1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.18662696C>G
CLNSRC ClinVar
CLNACC RCV000058878.1,