Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11552822
rs11552822
CDKN2A
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 GeneticVariation UNIPROT

dbSNP: rs747621669
rs747621669
CDKN2A
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 GeneticVariation UNIPROT