INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2059807
rs2059807
Entrez Id: 3643
Gene Symbol: INSR
INSR
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE Risk allele homozygotes (rs2059807) were less prevalent among subjects with obesity-related cancer. 26077721 2015