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: rs17208187
rs17208187
NDUFA2 ; TMCO6
5 140643653 missense variant C/G snv 0.24 0.20
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs778591
rs778591
IK ; NDUFA2 ; TMCO6 ; MIR3655
5 140645899 intron variant G/A snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs778593
rs778593
IK ; NDUFA2 ; TMCO6 ; MIR3655
5 140647631 5 prime UTR variant T/C snv 0.42 0.39
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs778601
rs778601
TMCO6
5 140620843 intergenic variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2569190
rs2569190
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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
CD14 ; TMCO6
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: rs2563298
rs2563298
CD14 ; TMCO6
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2014 2014
dbSNP: rs2563298
rs2563298
CD14 ; TMCO6
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2014 2014
dbSNP: rs2563298
rs2563298
CD14 ; TMCO6
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.010 1.000 1 2018 2018
dbSNP: rs2563298
rs2563298
CD14 ; TMCO6
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
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: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma 		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: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		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: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.010 < 0.001 1 2018 2018
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: C1719498
Disease: Generalized chronic periodontitis
Generalized chronic periodontitis 		0.010 1.000 1 2017 2017
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: 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: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis 		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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 < 0.001 1 2018 2018
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: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 < 0.001 1 2019 2019
dbSNP: rs2569190
rs2569190
CD14 ; TMCO6
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