SLC15A2, solute carrier family 15 member 2, 6565

N. diseases: 13; N. variants: 9
Disease: Multiple Sclerosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4285028
rs4285028
Entrez Id: 6565
Gene Symbol: SLC15A2
SLC15A2
CUI: C0026769
Disease:
Multiple Sclerosis 		0.800 GeneticVariation GWASCAT Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. 26920376 2016
dbSNP: rs4285028
rs4285028
Entrez Id: 6565
Gene Symbol: SLC15A2
SLC15A2
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs4285028
rs4285028
Entrez Id: 6565
Gene Symbol: SLC15A2
SLC15A2
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011