rs5361, SELE;C1orf112

N. diseases: 47
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.090 0.889 9 1997 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.080 0.875 8 2001 2011
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.070 1.000 7 1999 2019
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.070 1.000 7 1999 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.050 0.800 5 2003 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.040 0.750 4 1998 2014
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.030 1.000 3 2009 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.030 1.000 3 2003 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.030 1.000 3 2009 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 1.000 2 2013 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 1.000 2 2005 2009
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 0.500 2 2003 2007
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 1.000 2 2013 2016
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 1.000 2 2012 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 0.500 2 2010 2014
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 1.000 2 2007 2009
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 0.500 2 2010 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.020 1.000 2 2012 2013
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2014 2014
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2014 2014
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2009 2009
Arteriopathic disease
CUI: C0852949
Disease: Arteriopathic disease
14 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2004 2004
Asthma
CUI: C0004096
Disease: Asthma
1536 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2007 2007
Brucellosis
CUI: C0006309
Disease: Brucellosis
30 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2007 2007
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2016 2016