Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs920778
rs920778
HOTAIR
0.020 GeneticVariation BEFREE SNP rs920778 is also a useful risk factor in evaluation of Asian population and digestive cancer. 27965458

2017
dbSNP: rs920778
rs920778
HOTAIR
0.020 GeneticVariation BEFREE However, in further stratified analyses, the variant T allele of rs920778 exhibited a significant increased risk of developing digestive cancers (dominant model: OR = 1.44; 95% CI = 1.31-1.59). 27010768

2016