WDR35, WD repeat domain 35, 57539

N. diseases: 188; N. variants: 30
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607174
rs267607174
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3150874
Disease:
CRANIOECTODERMAL DYSPLASIA 2
C 0.800 CausalMutation CLINVAR
dbSNP: rs267607175
rs267607175
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3150874
Disease:
CRANIOECTODERMAL DYSPLASIA 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs431905505
rs431905505
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3279792
Disease:
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
0.800 GeneticVariation UNIPROT
dbSNP: rs431905505
rs431905505
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3279792
Disease:
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
G 0.800 CausalMutation CLINVAR
dbSNP: rs200140363
rs200140363
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0266449
Disease:
Congenital anomaly of brain
T 0.710 GeneticVariation CLINVAR
dbSNP: rs1050086118
rs1050086118
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0036996
Disease:
Short Rib-Polydactyly Syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1327489348
rs1327489348
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3279792
Disease:
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
TC 0.700 CausalMutation CLINVAR
dbSNP: rs1327489348
rs1327489348
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3150874
Disease:
CRANIOECTODERMAL DYSPLASIA 2
TC 0.700 CausalMutation CLINVAR
dbSNP: rs1553313859
rs1553313859
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3150874
Disease:
CRANIOECTODERMAL DYSPLASIA 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553316926
rs1553316926
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0265275
Disease:
Jeune thoracic dystrophy
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553317813
rs1553317813
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3150874
Disease:
CRANIOECTODERMAL DYSPLASIA 2
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553317813
rs1553317813
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3279792
Disease:
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553324519
rs1553324519
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3279792
Disease:
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
T 0.700 CausalMutation CLINVAR
dbSNP: rs1558342399
rs1558342399
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0036996
Disease:
Short Rib-Polydactyly Syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs199840434
rs199840434
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3150874
Disease:
CRANIOECTODERMAL DYSPLASIA 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs199840434
rs199840434
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3279792
Disease:
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
A 0.700 CausalMutation CLINVAR
dbSNP: rs199952377
rs199952377
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C4551571
Disease:
Cranioectodermal dysplasia
C 0.700 CausalMutation CLINVAR
dbSNP: rs199952377
rs199952377
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0265275
Disease:
Jeune thoracic dystrophy
C 0.700 CausalMutation CLINVAR
dbSNP: rs200140363
rs200140363
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C3150874
Disease:
CRANIOECTODERMAL DYSPLASIA 2
T 0.700 GeneticVariation CLINVAR
dbSNP: rs200140363
rs200140363
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C4021790
Disease:
Abnormality of the skeletal system
T 0.700 GeneticVariation CLINVAR
dbSNP: rs200649783
rs200649783
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0265275
Disease:
Jeune thoracic dystrophy
A 0.700 CausalMutation CLINVAR
dbSNP: rs200649783
rs200649783
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C4747658
Disease:
SHORT-RIB THORACIC DYSPLASIA 7/20 WITH POLYDACTYLY, DIGENIC
A 0.700 CausalMutation CLINVAR
dbSNP: rs200649783
rs200649783
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C0036996
Disease:
Short Rib-Polydactyly Syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs200649783
rs200649783
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C4694035
Disease:
SHORT-RIB THORACIC DYSPLASIA 7 WITHOUT POLYDACTYLY
A 0.700 CausalMutation CLINVAR
dbSNP: rs267607174
rs267607174
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
CUI: C4551571
Disease:
Cranioectodermal dysplasia
C 0.700 CausalMutation CLINVAR