rs886039814, WDR19

N. diseases: 13
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 GeneticVariation CLINVAR
Echogenic kidneys
CUI: C3549567
Disease: Echogenic kidneys
0.700 GeneticVariation CLINVAR
Cranioectodermal dysplasia
CUI: C4551571
Disease: Cranioectodermal dysplasia
0.700 GeneticVariation CLINVAR
Delayed myelination
CUI: C1277241
Disease: Delayed myelination
0.700 GeneticVariation CLINVAR
SENIOR-LOKEN SYNDROME 8
CUI: C4225376
Disease: SENIOR-LOKEN SYNDROME 8
0.700 GeneticVariation CLINVAR
Dysmorphic facies
CUI: C0424503
Disease: Dysmorphic facies
0.700 GeneticVariation CLINVAR
Microcephaly (physical finding)
CUI: C4551563
Disease: Microcephaly (physical finding)
0.700 GeneticVariation CLINVAR
Short extremities
CUI: C0239399
Disease: Short extremities
0.700 GeneticVariation CLINVAR
Diastrophic dysplasia
CUI: C0220726
Disease: Diastrophic dysplasia
0.700 GeneticVariation CLINVAR
Small eyes
CUI: C1837464
Disease: Small eyes
0.700 GeneticVariation CLINVAR
Syndactyly, type 2
CUI: C2699746
Disease: Syndactyly, type 2
0.700 GeneticVariation CLINVAR
Caroli Disease
CUI: C0162510
Disease: Caroli Disease
0.700 GeneticVariation CLINVAR
Keratosis Follicularis
CUI: C0022595
Disease: Keratosis Follicularis
0.700 GeneticVariation CLINVAR