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: rs908247294
rs908247294
CRP
1.000 0.040 1 159713626 missense variant T/C snv 4.0E-06
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease 		0.010 1.000 1 2020 2020
dbSNP: rs77832441
rs77832441
CRP
0.882 0.040 1 159714024 missense variant G/A snv 1.4E-03 1.6E-03
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 < 0.001 1 2015 2015
dbSNP: rs77832441
rs77832441
CRP
0.882 0.040 1 159714024 missense variant G/A snv 1.4E-03 1.6E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 < 0.001 1 2015 2015
dbSNP: rs77832441
rs77832441
CRP
0.882 0.040 1 159714024 missense variant G/A snv 1.4E-03 1.6E-03
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 < 0.001 1 2015 2015
dbSNP: rs774679649
rs774679649
CRP
1 159713878 missense variant T/C snv 4.0E-06 7.0E-06
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2009 2009
dbSNP: rs756067092
rs756067092
CRP
1.000 0.120 1 159713823 missense variant T/C snv 4.0E-06
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2010 2010
dbSNP: rs748954737
rs748954737
CRP
0.882 0.040 1 159713734 missense variant C/T snv 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2006 2006
dbSNP: rs748954737
rs748954737
CRP
0.882 0.040 1 159713734 missense variant C/T snv 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2006 2006
dbSNP: rs748954737
rs748954737
CRP
0.882 0.040 1 159713734 missense variant C/T snv 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2006 2006
dbSNP: rs3093061
rs3093061
CRP
0.851 0.160 1 159715192 upstream gene variant T/C snv 4.8E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.020 1.000 2 2008 2018
dbSNP: rs3093061
rs3093061
CRP
0.851 0.160 1 159715192 upstream gene variant T/C snv 4.8E-02
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris 		0.010 1.000 1 2018 2018
dbSNP: rs3093061
rs3093061
CRP
0.851 0.160 1 159715192 upstream gene variant T/C snv 4.8E-02
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid 		0.010 1.000 1 2018 2018
dbSNP: rs3093061
rs3093061
CRP
0.851 0.160 1 159715192 upstream gene variant T/C snv 4.8E-02
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus 		0.010 1.000 1 2018 2018
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.050 1.000 5 2013 2020
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 3 2011 2019
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.020 1.000 2 2014 2015
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.020 1.000 2 2014 2015
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2008 2008
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia 		0.010 1.000 1 2017 2017
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.010 1.000 1 2016 2016
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		0.010 1.000 1 2009 2009
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2013 2013
dbSNP: rs3093059
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13
CUI: C0497327
Disease: Dementia
Dementia 		0.010 1.000 1 2016 2016
dbSNP: rs3093058
rs3093058
CRP
1 159715525 upstream gene variant T/A;C;G snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2012 2012