rs1050086118
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Short Rib-Polydactyly Syndrome
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1050086118
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia.
|
28400947 |
2017 |
rs113386058
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Waist-Hip Ratio
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs1327489348
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
TC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1327489348
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
CRANIOECTODERMAL DYSPLASIA 2
|
TC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1381817
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Lymphocyte Count measurement
|
|
0.700 |
GeneticVariation |
GWASDB |
The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.
|
22286170 |
2012 |
rs1553313859
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
CRANIOECTODERMAL DYSPLASIA 2
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1553316926
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Jeune thoracic dystrophy
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1553317813
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
CRANIOECTODERMAL DYSPLASIA 2
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1553317813
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1553324519
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1558342399
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Short Rib-Polydactyly Syndrome
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1558342399
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia.
|
28400947 |
2017 |
rs199840434
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
CRANIOECTODERMAL DYSPLASIA 2
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs199840434
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Cranioectodermal dysplasia
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Cranioectodermal dysplasia
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations.
|
28332779 |
2017 |
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Cranioectodermal dysplasia
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.
|
25914204 |
2015 |
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
C |
0.700 |
CausalMutation |
CLINVAR |
Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome).
|
22486404 |
2013 |
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
Jeune thoracic dystrophy
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
CRANIOECTODERMAL DYSPLASIA 2
|
C |
0.700 |
CausalMutation |
CLINVAR |
Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome).
|
22486404 |
2013 |
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
CRANIOECTODERMAL DYSPLASIA 2
|
C |
0.700 |
CausalMutation |
CLINVAR |
Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations.
|
28332779 |
2017 |
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
CRANIOECTODERMAL DYSPLASIA 2
|
C |
0.700 |
CausalMutation |
CLINVAR |
Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.
|
25914204 |
2015 |
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
C |
0.700 |
CausalMutation |
CLINVAR |
Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations.
|
28332779 |
2017 |
rs199952377
|
Entrez Id: |
57539 |
Gene Symbol: |
WDR35 |
WDR35
|
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
|
C |
0.700 |
CausalMutation |
CLINVAR |
Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.
|
25914204 |
2015 |