rs2890565, UTS2

N. diseases: 15
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.
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.020 1.000 2 2003 2004
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.020 1.000 2 2016 2017
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2016 2016
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2013 2013
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2015 2015
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2016 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2012 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2012 2012
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2012 2012
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1 2010 2010
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2007 2007
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2015 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2009 2009
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 0.010 1.000 1 2012 2012