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: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic
0.700 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: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
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: 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: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
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: 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: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura
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: 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: C0010068
Disease: Coronary heart disease
Coronary heart disease
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: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic 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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2014 2014
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: 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: C0019196
Disease: Hepatitis C
Hepatitis C
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: 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: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
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: C0151281
Disease: Genital ulcers
Genital ulcers
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: C0684249
Disease: Carcinoma of lung
Carcinoma 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: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
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: C0004096
Disease: Asthma
Asthma
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: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
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: 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: 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: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome
0.010 < 0.001 1 2017 2017