rs1799983, NOS3

N. diseases: 246
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2019 2019
Dengue Fever
CUI: C0011311
Disease: Dengue Fever
39 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2019 2019
Kidney Calculi
CUI: C0022650
Disease: Kidney Calculi
71 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2019 2019
Left-Sided Heart Failure
CUI: C0023212
Disease: Left-Sided Heart Failure
5 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2019 2019
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2019 2019
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2019 2019
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2019 2019
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
105 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2019 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Ataxia with vitamin E deficiency
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
32 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Carcinoma of urinary bladder, invasive
CUI: C1827293
Disease: Carcinoma of urinary bladder, invasive
14 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Oligoasthenozoospermia
CUI: C3164407
Disease: Oligoasthenozoospermia
6 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Peripheral arterial stenosis
CUI: C4025272
Disease: Peripheral arterial stenosis
5 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Spindle cell hemangioma
CUI: C1304508
Disease: Spindle cell hemangioma
10 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Mycoplasma pneumonia
CUI: C0032302
Disease: Mycoplasma pneumonia
2 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2017 2017
Otitis Media with Effusion
CUI: C0029883
Disease: Otitis Media with Effusion
1 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2017 2017
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2016 2016
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2016 2016
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2016 2016
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2016 2016