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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.641 0.600 6 31572536 intron variant A/G;T snv 0.700 0
PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO (finding)
1 0.641 0.600 6 31572536 intron variant A/G;T snv 0.700 0
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2009 2009
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2009 2009
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
14 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2009 2009
Asthma
CUI: C0004096
Disease: Asthma
1536 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.641 0.600 6 31572536 intron variant A/G;T snv 0.020 0.500 2 2006 2013
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2013 2013
Malignant Childhood Neoplasm
CUI: C0278704
Disease: Malignant Childhood Neoplasm
34 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2013 2013
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2013 2013
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2013 2013
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
60 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Migraine with Aura
CUI: C0154723
Disease: Migraine with Aura
56 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
14 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2015 2015
Influenza A
CUI: C2062441
Disease: Influenza A
19 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2015 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2015 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2015 2015
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2016 2016
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2016 2016
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2017 2017