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: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.030 1.000 3 2010 2019
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.060 0.833 6 2015 2019
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2008 2008
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
0.010 1.000 1 2011 2011
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2011 2011
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2015 2015
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2017 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.010 1.000 1 2018 2018
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome
0.010 < 0.001 1 2017 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.040 1.000 4 2010 2015
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.010 < 0.001 1 2017 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2019 2019
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0027873
Disease: Neuromyelitis Optica
Neuromyelitis Optica
0.010 1.000 1 2017 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.010 1.000 1 2017 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0029453
Disease: Osteopenia
Osteopenia
0.010 1.000 1 2008 2008
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 1.000 1 2008 2008
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2015 2015
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C2937365
Disease: Recurrent aphthous ulcer
Recurrent aphthous ulcer
0.010 1.000 1 2017 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.730 0.750 4 2012 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.020 < 0.001 2 2011 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2018 2018
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 1.000 1 2018 2018
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.010 < 0.001 1 2017 2017
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
0.010 1.000 1 2019 2019