Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs641738
rs641738
MBOAT7 ; TMC4 ; LOC112268246
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.020 GeneticVariation BEFREE Studies found a mutation on MBOAT7, rs641738 and another on TM6SF2, rs58542926 were associated with liver diseases, including NAFLD. 30824369

2019
dbSNP: rs641738
rs641738
MBOAT7 ; TMC4 ; LOC112268246
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.020 GeneticVariation BEFREE Furthermore, multivariable logistic regression analysis adjusted for biologically relevant covariates and potential confounders associated with the risk of liver disease progression revealed that MBOAT7 rs641738 is not associated either with fibrosis progression in CHC group (OR = 1.12; 95% CI: 0.55-2.28; p = 0.761) or with chronic progressive state in CHB patients (OR = 0.81; 95% CI: 0.41-1.61; p = 0.547). 30116012

2018