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rs199469695

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199469695(G;G)
Make rs199469695(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position18644578
GeneCDKL5, RS1
is asnp
is mentioned by
dbSNPrs199469695
ebirs199469695
HLIrs199469695
Exacrs199469695
Varsomers199469695
Maprs199469695
PheGenIrs199469695
hapmaprs199469695
1000 genomesrs199469695
hgdprs199469695
ensemblrs199469695
gopubmedrs199469695
geneviewrs199469695
scholarrs199469695
googlers199469695
pharmgkbrs199469695
gwascentralrs199469695
openSNPrs199469695
23andMers199469695
23andMe allrs199469695
SNP Nexus

SNPshotrs199469695
SNPdbers199469695
MSV3drs199469695
GWAS Ctlgrs199469695
Max Magnitude0
ClinVar
Risk rs199469695(G;G)
Alt rs199469695(G;G)
Reference rs199469695(T;T)
Significance Untested
Disease not provided
Variation info
Gene CDKL5 RS1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.18662698A>C
CLNSRC ClinVar
CLNACC RCV000058877.1,