LMAN1, lectin, mannose binding 1, 3998

N. diseases: 30; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2298711
rs2298711
Entrez Id: 3998
Gene Symbol: LMAN1
LMAN1
CUI: C0883409
Disease:
Cardiac troponin I measurement 		A 0.700 GeneticVariation GWASCAT Cardiac Troponin T and Troponin I in the General Population. 31014085 2019
dbSNP: rs121909253
rs121909253
Entrez Id: 3998
Gene Symbol: LMAN1
LMAN1
CUI: C4551981
Disease:
Familial Multiple Coagulation Factor Deficiency I 		G 0.700 CausalMutation CLINVAR
dbSNP: rs869312030
rs869312030
Entrez Id: 3998
Gene Symbol: LMAN1
LMAN1
CUI: C4551981
Disease:
Familial Multiple Coagulation Factor Deficiency I 		GC 0.700 CausalMutation CLINVAR
dbSNP: rs869312031
rs869312031
Entrez Id: 3998
Gene Symbol: LMAN1
LMAN1
CUI: C4551981
Disease:
Familial Multiple Coagulation Factor Deficiency I 		G 0.700 CausalMutation CLINVAR
dbSNP: rs869312032
rs869312032
Entrez Id: 3998
Gene Symbol: LMAN1
LMAN1
CUI: C4551981
Disease:
Familial Multiple Coagulation Factor Deficiency I 		T 0.700 CausalMutation CLINVAR
dbSNP: rs869312033
rs869312033
Entrez Id: 3998
Gene Symbol: LMAN1
LMAN1
CUI: C4551981
Disease:
Familial Multiple Coagulation Factor Deficiency I 		A 0.700 CausalMutation CLINVAR