Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1420472625
rs1420472625
MBOAT7
0.040 GeneticVariation BEFREE In non-obese NAFLD patients, the frequency of the PNPLA3 p.I148M allele (74.6%), but not of the TM6SF2 or MBOAT7 polymorphisms, was significantly (P < 0.05) higher as compared to the other patients in the NAFLD CSG cohort (54.9%) or controls (40.2%). 29483677

2018
dbSNP: rs1420472625
rs1420472625
MBOAT7
0.040 GeneticVariation BEFREE Notably, the I148M PNPLA3 variant has been identified as the major common genetic determinant of NAFLD. 29122391

2018
dbSNP: rs1420472625
rs1420472625
MBOAT7
0.040 GeneticVariation BEFREE The PNPLA3 p.I148M, TM6SF2 p.E167K, and MBOAT7 rs641738 variants represent genetic risk factors for nonalcoholic fatty liver disease (NAFLD). 27836992

2017
dbSNP: rs1420472625
rs1420472625
MBOAT7
0.040 GeneticVariation BEFREE NAFLD is further favored by the patatin-like phospholipase domain-containing 3 (PNPLA3) p.I148M, transmembrane 6 superfamily member 2 (TM6SF2) p.E167K, and membrane-bound O-acyltransferase domain containing 7 (MBOAT7) rs641738 variants. 27576208

2016