Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.020 GeneticVariation BEFREE The C282Y and H63D HFE variants frequencies were determined in 373 patients with MS and compared with a normal population. 20586792

2011
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.020 GeneticVariation BEFREE One C282Y-homozygous female was identified who had MS and was being treated for symptoms of iron overload. 15014978

2004