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: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2013 2013
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
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: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		0.010 1.000 1 2018 2018
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		0.010 1.000 1 2015 2015
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2014 2014
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2017 2017
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2009 2009
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0014121
Disease: Bacterial Endocarditis
Bacterial Endocarditis 		0.010 1.000 1 2017 2017
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C1541923
Disease: Infective endocarditis
Infective endocarditis 		0.010 1.000 1 2017 2017
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0564567
Disease: Impulsive character (finding)
Impulsive character (finding) 		0.010 1.000 1 2013 2013
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris 		0.010 1.000 1 2018 2018
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.010 1.000 1 2018 2018
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.010 1.000 1 2010 2010
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid 		0.010 1.000 1 2018 2018
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2010 2010
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2010 2010
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		0.010 1.000 1 2018 2018
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2008 2008
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus 		0.010 1.000 1 2018 2018
dbSNP: rs1130864
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		0.010 1.000 1 2017 2017
dbSNP: rs1205
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs1205
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.010 1.000 1 2017 2017
dbSNP: rs1205
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		0.010 1.000 1 2009 2009