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: C0031099
Disease: Periodontitis
Periodontitis
0.030 0.667 3 2016 2019
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.020 1.000 2 2009 2019
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0004096
Disease: Asthma
Asthma
0.020 1.000 2 2011 2012
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0243026
Disease: Sepsis
Sepsis
0.020 1.000 2 2014 2015
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0036690
Disease: Septicemia
Septicemia
0.020 1.000 2 2014 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
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0947961
Disease: Atopic disorders
Atopic disorders
0.010 1.000 1 2005 2005
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.010 1.000 1 2009 2009
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0277528
Disease: Traveler's diarrhea
Traveler's diarrhea
0.010 1.000 1 2011 2011
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis
0.010 1.000 1 2014 2014
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
Congenital atresia of extrahepatic bile duct
0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.010 1.000 1 2014 2014
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0010068
Disease: Coronary heart disease
Coronary heart 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: C3662483
Disease: Allergic sensitization
Allergic sensitization
0.010 1.000 1 2010 2010
dbSNP: rs2569190
rs2569190
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2020 2020
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