INS, insulin, 3630

N. diseases: 405; N. variants: 37
Disease: Adenocarcinoma of the gastroesophageal junction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs689
rs689
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1332166
Disease:
Adenocarcinoma of the gastroesophageal junction 		0.010 GeneticVariation BEFREE Our findings highlight that TCF7L2 rs290481, INS rs689, and INSR rs1799817 polymorphisms may increase the risk of AEG. 31211453 2019