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: rs3110697
rs3110697
0.827 0.160 7 45915430 intron variant A/G snv 0.58
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs3110697
rs3110697
0.827 0.160 7 45915430 intron variant A/G snv 0.58
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2007 2007
dbSNP: rs3110697
rs3110697
0.827 0.160 7 45915430 intron variant A/G snv 0.58
CUI: C0016034
Disease: Breast Fibrocystic Disease
Breast Fibrocystic Disease
0.010 1.000 1 2010 2010
dbSNP: rs3110697
rs3110697
0.827 0.160 7 45915430 intron variant A/G snv 0.58
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs3110697
rs3110697
0.827 0.160 7 45915430 intron variant A/G snv 0.58
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs3110697
rs3110697
0.827 0.160 7 45915430 intron variant A/G snv 0.58
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2017 2017