Source: ALL

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: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.010 < 0.001 1 2018 2018
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 < 0.001 1 2018 2018
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0155877
Disease: Allergic asthma
Allergic asthma
0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2013 2013
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2020 2020
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2017 2017
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1719498
Disease: Generalized chronic periodontitis
Generalized chronic periodontitis
0.010 1.000 1 2017 2017
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia
0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.010 1.000 1 2010 2010
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis
0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis
0.010 1.000 1 2016 2016
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.010 1.000 1 2016 2016
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C4554344
Disease: IgE-mediated food allergy
IgE-mediated food allergy
0.010 1.000 1 2019 2019
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0035243
Disease: Respiratory Tract Infections
Respiratory Tract Infections
0.010 1.000 1 2017 2017
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 < 0.001 1 2019 2019
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0013595
Disease: Eczema
Eczema
0.010 1.000 1 2005 2005
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
0.010 1.000 1 2019 2019
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract
0.010 1.000 1 2016 2016
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 1.000 1 2014 2014
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2019 2019