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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.730 1.000 5 2010 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.730 1.000 5 2010 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.010 1 2015 2015
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.010 1 2012 2012
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.010 1 2015 2015