Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs758900778
rs758900778
0.010 GeneticVariation BEFREE We previously demonstrated a haplotype variant c.53C>T/c.74G>A of hMYH (T/A) increasing the risk for gastric cancer in Chinese. 18811933

2008

dbSNP: rs79777494
rs79777494
0.010 GeneticVariation BEFREE We previously demonstrated a haplotype variant c.53C>T/c.74G>A of hMYH (T/A) increasing the risk for gastric cancer in Chinese. 18811933

2008