Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918714
rs121918714
TGFBR2
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.710 GeneticVariation UNIPROT

dbSNP: rs121912967
rs121912967
DCC
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs3829868
rs3829868
CRNN ; FLG-AS1
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.700 GeneticVariation UNIPROT