CDC42, cell division cycle 42, 998

N. diseases: 327; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864309721
rs864309721
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4225222
Disease:
TAKENOUCHI-KOSAKI SYNDROME 		G 0.820 CausalMutation CLINVAR
dbSNP: rs864309721
rs864309721
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4225222
Disease:
TAKENOUCHI-KOSAKI SYNDROME 		G 0.820 GeneticVariation CLINVAR
dbSNP: rs1064795845
rs1064795845
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4225222
Disease:
TAKENOUCHI-KOSAKI SYNDROME 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196096
rs1553196096
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C1843367
Disease:
Poor school performance 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1553196096
rs1553196096
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C1859778
Disease:
Postnatal growth retardation 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1553196096
rs1553196096
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4021866
Disease:
obsolete Abnormal heart morphology 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1553196096
rs1553196096
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0040034
Disease:
Thrombocytopenia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1553196096
rs1553196096
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0424503
Disease:
Dysmorphic facies 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1553196100
rs1553196100
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4225222
Disease:
TAKENOUCHI-KOSAKI SYNDROME 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4021085
Disease:
Abnormality of brain morphology 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C1859778
Disease:
Postnatal growth retardation 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0038379
Disease:
Strabismus 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C3806482
Disease:
Recurrent respiratory infections 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0036572
Disease:
Seizures 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4225222
Disease:
TAKENOUCHI-KOSAKI SYNDROME 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0424503
Disease:
Dysmorphic facies 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196101
rs1553196101
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C1843367
Disease:
Poor school performance 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553196134
rs1553196134
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4021085
Disease:
Abnormality of brain morphology 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553196134
rs1553196134
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C1859778
Disease:
Postnatal growth retardation 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553196134
rs1553196134
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0038379
Disease:
Strabismus 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553196134
rs1553196134
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0028866
Disease:
Oculomotor Nerve Paralysis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553196134
rs1553196134
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C0424503
Disease:
Dysmorphic facies 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553196134
rs1553196134
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C1843367
Disease:
Poor school performance 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553196539
rs1553196539
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4225222
Disease:
TAKENOUCHI-KOSAKI SYNDROME 		A 0.700 CausalMutation CLINVAR
dbSNP: rs797044870
rs797044870
Entrez Id: 998
Gene Symbol: CDC42
CDC42
CUI: C4225222
Disease:
TAKENOUCHI-KOSAKI SYNDROME 		G 0.700 CausalMutation CLINVAR