LRRC56, leucine rich repeat containing 56, 115399

N. diseases: 45; N. variants: 33
Disease: CILIARY DYSKINESIA, PRIMARY, 39 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1564800859
rs1564800859
Entrez Id: 115399
Gene Symbol: LRRC56
LRRC56
CUI: C4748841
Disease:
CILIARY DYSKINESIA, PRIMARY, 39 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1564805039
rs1564805039
Entrez Id: 115399
Gene Symbol: LRRC56
LRRC56
CUI: C4748841
Disease:
CILIARY DYSKINESIA, PRIMARY, 39 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1564805053
rs1564805053
Entrez Id: 115399
Gene Symbol: LRRC56
LRRC56
CUI: C4748841
Disease:
CILIARY DYSKINESIA, PRIMARY, 39 		A 0.700 CausalMutation CLINVAR
dbSNP: rs372959912
rs372959912
Entrez Id: 115399
Gene Symbol: LRRC56
LRRC56
CUI: C4748841
Disease:
CILIARY DYSKINESIA, PRIMARY, 39 		T 0.700 CausalMutation CLINVAR