Variant: rs2235776 

    present in Gene: SAMM50
    present in Chromosome: 22
    Position on Chromosome: 43982119
    Alleles of this Variant: C/T

rs2235776 in SAMM50 gene and Fatty Liver Disease PMID 23477746 2013 The ERLIN1-CHUK-CWF19L1 gene cluster influences liver fat deposition and hepatic inflammation in the NHLBI Family Heart Study.

rs2235776 in SAMM50 gene and Non-alcoholic Fatty Liver Disease PMID 22719876 2012 Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese.

rs2235776 in SAMM50 gene and Serum total cholesterol measurement PMID 26780889 2016 Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.