SLC22A6, solute carrier family 22 member 6, 9356

N. diseases: 19; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs148838714
rs148838714
Entrez Id: 9356
Gene Symbol: SLC22A6
SLC22A6
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019