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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C4520983
Disease: Congenital atresia of extrahepatic bile duct
Congenital atresia of extrahepatic bile duct 		0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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