AFP, alpha fetoprotein, 174

N. diseases: 392; N. variants: 9
Disease: Cirrhosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10020432
rs10020432
Entrez Id: 174
Gene Symbol: AFP
AFP
CUI: C1623038
Disease:
Cirrhosis 		0.010 GeneticVariation BEFREE Furthermore, we identified two SNPs in AFP intron 7 and 3'UTR, rs2298839 and rs10020432, which are associated with increased risk of cirrhosis. 19968979 2010
dbSNP: rs2298839
rs2298839
Entrez Id: 174
Gene Symbol: AFP
AFP
CUI: C1623038
Disease:
Cirrhosis 		0.010 GeneticVariation BEFREE Furthermore, we identified two SNPs in AFP intron 7 and 3'UTR, rs2298839 and rs10020432, which are associated with increased risk of cirrhosis. 19968979 2010
dbSNP: rs6834059
rs6834059
Entrez Id: 174
Gene Symbol: AFP
AFP
CUI: C1623038
Disease:
Cirrhosis 		0.010 GeneticVariation BEFREE Statistically significant associations with HCC and cirrhosis were detected for six individual SNPs in the AFP promoter, AFP intron 1 and intron 2 (rs6834059, rs3796678, rs3796677, rs3796676, rs28532518 and rs4646038). 19968979 2010