rs751375244, TRAPPC3

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Diastrophic dysplasia
CUI: C0220726
Disease: Diastrophic dysplasia
0.700 GeneticVariation CLINVAR
Bardet-Biedl Syndrome
CUI: C0752166
Disease: Bardet-Biedl Syndrome
0.700 GeneticVariation CLINVAR
Keratosis Follicularis
CUI: C0022595
Disease: Keratosis Follicularis
0.700 GeneticVariation CLINVAR
Melanocortin 4 Receptor Deficiency
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
0.700 GeneticVariation CLINVAR
Polydactyly
CUI: C0152427
Disease: Polydactyly
0.700 GeneticVariation CLINVAR
Low Vision
CUI: C0042798
Disease: Low Vision
0.700 GeneticVariation CLINVAR