rs236918, PCSK7

N. diseases: 10
Disease: Cirrhosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
0.030 GeneticVariation BEFREE We evaluated the associations between the PNPLA3 (rs738409), RNF7 (rs16851720), MERTK (rs4374383) and PCSK7 (rs236918) variants and liver fibrosis and cirrhosis in a series of consecutive patients recruited at the Department of Gastroenterology, Lithuanian University of Health Sciences Hospital, during the period 2012-2015. 28338112 2017
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
0.030 GeneticVariation BEFREE These findings confirm that PCSK7 rs236918 C allele is a risk factor for cirrhosis development in Italian patients with HFE-Hemochromatosis. 26868056 2016
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
0.030 GeneticVariation BEFREE PCSK7 variant rs236918</span> is a risk factor for cirrhosis in HH patients homozygous for the HFE C282Y mutation. 24556216 2014