Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1063169
rs1063169
Entrez Id: 2353
Gene Symbol: FOS
FOS
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The rs7101 and rs1063169 polymorphisms in the noncoding region of FOS are associated with the risk of developing colorectal cancer and the progression of colorectal cancer, which may be because the mutation enhances the expression of c-Fos protein to promote the incidence and development of colorectal cancer. 31261535 2019
dbSNP: rs1063169
rs1063169
Entrez Id: 2353
Gene Symbol: FOS
FOS
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE The rs7101 and rs1063169 polymorphisms in the noncoding region of FOS are associated with the risk of developing colorectal cancer and the progression of colorectal cancer, which may be because the mutation enhances the expression of c-Fos protein to promote the incidence and development of colorectal cancer. 31261535 2019
dbSNP: rs7101
rs7101
Entrez Id: 2353
Gene Symbol: FOS
FOS
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE The rs7101 and rs1063169 polymorphisms in the noncoding region of FOS are associated with the risk of developing colorectal cancer and the progression of colorectal cancer, which may be because the mutation enhances the expression of c-Fos protein to promote the incidence and development of colorectal cancer. 31261535 2019
dbSNP: rs7101
rs7101
Entrez Id: 2353
Gene Symbol: FOS
FOS
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The rs7101 and rs1063169 polymorphisms in the noncoding region of FOS are associated with the risk of developing colorectal cancer and the progression of colorectal cancer, which may be because the mutation enhances the expression of c-Fos protein to promote the incidence and development of colorectal cancer. 31261535 2019
dbSNP: rs750949764
rs750949764
Entrez Id: 2353
Gene Symbol: FOS
FOS
CUI: C0206732
Disease:
Epithelioid hemangioendothelioma
0.010 GeneticVariation BEFREE Whereas, deleterious variants, especially PTPN11 c.226G>A, may be linked to tumorigenesis of AS. 29206716 2018
dbSNP: rs750949764
rs750949764
Entrez Id: 2353
Gene Symbol: FOS
FOS
CUI: C0596263
Disease:
Carcinogenesis
0.010 GeneticVariation BEFREE Whereas, deleterious variants, especially PTPN11 c.226G>A, may be linked to tumorigenesis of AS. 29206716 2018