Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11466537
rs11466537
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C1515091
Disease:
Surgically-Created Resection Cavity
0.010 GeneticVariation BEFREE Our results demonstrated that hsa-miR-1193 may be involved in sCRC tumourigenesis at least in part by suppression of TGFBR2, and the A allele of rs11466537 disturbed the regulation of hsa-miR-1193 on TGFBR2. 28494187 2017