CDKL5, cyclin dependent kinase like 5, 6792

N. diseases: 224; N. variants: 221
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267608479
rs267608479
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs267608650
rs267608650
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs267608657
rs267608657
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 GeneticVariation CLINVAR
dbSNP: rs61750250
rs61750250
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs62641235
rs62641235
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs62643614
rs62643614
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs786204975
rs786204975
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs786204976
rs786204976
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs786204984
rs786204984
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs786204986
rs786204986
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
A 0.700 CausalMutation CLINVAR
dbSNP: rs267608623
rs267608623
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
AC 0.700 CausalMutation CLINVAR
dbSNP: rs786204988
rs786204988
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
AGT 0.700 CausalMutation CLINVAR
dbSNP: rs267608430
rs267608430
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
C 0.700 CausalMutation CLINVAR
dbSNP: rs267608433
rs267608433
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
C 0.700 CausalMutation CLINVAR
dbSNP: rs61753251
rs61753251
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
C 0.700 CausalMutation CLINVAR
dbSNP: rs62643608
rs62643608
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
C 0.700 CausalMutation CLINVAR
dbSNP: rs786204963
rs786204963
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
C 0.700 GeneticVariation CLINVAR
dbSNP: rs786204972
rs786204972
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
C 0.700 CausalMutation CLINVAR
dbSNP: rs786204970
rs786204970
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
CA 0.700 CausalMutation CLINVAR
dbSNP: rs267608646
rs267608646
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
CAT 0.700 CausalMutation CLINVAR
dbSNP: rs267608468
rs267608468
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
G 0.700 GeneticVariation CLINVAR
dbSNP: rs587783072
rs587783072
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
G 0.700 GeneticVariation CLINVAR
dbSNP: rs786204992
rs786204992
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
G 0.700 CausalMutation CLINVAR
dbSNP: rs122460157
rs122460157
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
T 0.700 CausalMutation CLINVAR
dbSNP: rs122460158
rs122460158
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5
CUI: C2748910
Disease:
Rett Syndrome, Atypical
T 0.700 CausalMutation CLINVAR