rs10931936, CASP8

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.827 0.120 2 201279205 intron variant T/C snv 0.72 0.710 1.000 2 2012 2017
melanoma
CUI: C0025202
Disease: melanoma
515 0.827 0.120 2 201279205 intron variant T/C snv 0.72 0.700 1.000 1 2011 2011
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.827 0.120 2 201279205 intron variant T/C snv 0.72 0.020 0.500 2 2012 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.827 0.120 2 201279205 intron variant T/C snv 0.72 0.020 0.500 2 2012 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.827 0.120 2 201279205 intron variant T/C snv 0.72 0.010 1.000 1 2017 2017
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.827 0.120 2 201279205 intron variant T/C snv 0.72 0.010 1.000 1 2017 2017