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: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.010 1.000 1 2015 2015
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
androgen independent prostate cancer
0.010 1.000 1 2007 2007
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0002871
Disease: Anemia
Anemia
0.010 1.000 1 2013 2013
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2008 2008
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System
0.010 1.000 1 2014 2014
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2017 2017
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 1.000 2 2014 2014
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 1.000 2 2014 2014
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2017 2017
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
Conventional (Clear Cell) Renal Cell Carcinoma
0.030 1.000 3 2008 2018
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 < 0.001 1 2011 2011
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 1.000 1 2015 2015
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0011847
Disease: Diabetes
Diabetes
0.020 1.000 2 2013 2019
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.020 1.000 2 2013 2019
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.020 1.000 2 2005 2009
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer
0.010 1.000 1 2015 2015
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.030 1.000 3 2013 2019
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.010 1.000 1 2019 2019
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0013537
Disease: Eclampsia
Eclampsia
0.020 1.000 2 2008 2012
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.010 1.000 1 2016 2016
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0085119
Disease: Foot Ulcer
Foot Ulcer
0.010 1.000 1 2015 2015
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.010 1.000 1 2010 2010
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 1.000 1 2014 2014
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.010 1.000 1 2019 2019