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rs199469700

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs199469700(-;C)
Make rs199469700(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position18642015
GeneCDKL5, RS1
is asnp
is mentioned by
dbSNPrs199469700
dbSNP (classic)rs199469700
ClinGenrs199469700
ebirs199469700
HLIrs199469700
Exacrs199469700
Gnomadrs199469700
Varsomers199469700
LitVarrs199469700
Maprs199469700
PheGenIrs199469700
Biobankrs199469700
1000 genomesrs199469700
hgdprs199469700
ensemblrs199469700
geneviewrs199469700
scholarrs199469700
googlers199469700
pharmgkbrs199469700
gwascentralrs199469700
openSNPrs199469700
23andMers199469700
SNPshotrs199469700
SNPdbers199469700
MSV3drs199469700
GWAS Ctlgrs199469700
Max Magnitude0
ClinVar
Risk rs199469700(C;C)
Alt rs199469700(C;C)
Reference Rs199469700(-;-)
Significance Untested
Disease not provided
Variation info
Gene CDKL5 RS1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.18660136dupG
CLNSRC ClinVar
CLNACC RCV000058882.1,