rs758522600, BBS10

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
BARDET-BIEDL SYNDROME 10
CUI: C1859568
Disease: BARDET-BIEDL SYNDROME 10
0.700 GeneticVariation CLINVAR Characterizing the morbid genome of ciliopathies. 27894351 2016
Asphyxiating Thoracic Dystrophy 1
CUI: C4551856
Disease: Asphyxiating Thoracic Dystrophy 1
0.700 CausalMutation CLINVAR
Polydactyly
CUI: C0152427
Disease: Polydactyly
0.700 CausalMutation CLINVAR
Polycystic Kidney Diseases
CUI: C0022680
Disease: Polycystic Kidney Diseases
0.700 CausalMutation CLINVAR
Chylous Ascites
CUI: C0008732
Disease: Chylous Ascites
0.700 CausalMutation CLINVAR
Narrow thorax
CUI: C0426790
Disease: Narrow thorax
0.700 CausalMutation CLINVAR
Short ribs
CUI: C0426817
Disease: Short ribs
0.700 CausalMutation CLINVAR