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: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.060 0.833 6 2008 2018
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.020 1.000 2 2004 2009
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.020 1.000 2 2012 2012
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.020 1.000 2 2004 2009
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.020 1.000 2 2004 2009
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.020 1.000 2 2013 2015
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.010 1.000 1 2012 2012
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2016 2016
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.010 1.000 1 2011 2011
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.010 1.000 1 2011 2011
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
Cervical Squamous Cell Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2008 2008
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
0.010 1.000 1 2019 2019
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2008 2008
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2012 2012
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0206677
Disease: Adenomatous Polyps
Adenomatous Polyps
0.010 1.000 1 2015 2015