Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80358222
rs80358222
SLC16A1
0.800 GeneticVariation UNIPROT

dbSNP: rs80358222
rs80358222
SLC16A1
C 0.800 CausalMutation CLINVAR

dbSNP: rs72552271
rs72552271
SLC16A1
0.700 GeneticVariation UNIPROT Mutations in MCT1 cDNA in patients with symptomatic deficiency in lactate transport. 10590411

2000