Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6013897
rs6013897 		0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2012 2017
dbSNP: rs6013897
rs6013897 		0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.010 1.000 1 2019 2019
dbSNP: rs6013897
rs6013897 		0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs6013897
rs6013897 		0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs6013897
rs6013897 		0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid 		0.010 1.000 1 2019 2019
dbSNP: rs6013897
rs6013897 		0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs6013897
rs6013897 		0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2012 2012