Source: CURATED

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: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.800 1.000 4 2008 2016
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 2 2007 2010
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.800 1.000 1 2011 2011
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis
0.710 1.000 1 2014 2014
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 3 2007 2011
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 2 2009 2012
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0238067
Disease: Colitis, Collagenous
Colitis, Collagenous
0.700 1.000 1 2017 2017
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.700 1.000 1 2012 2012
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2016 2016
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2009 2009
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2016 2016
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2010 2010
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0202083
Disease: Immunoglobulin A measurement
Immunoglobulin A measurement
0.700 1.000 1 2010 2010
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0024137
Disease: Lupus Erythematosus, Cutaneous
Lupus Erythematosus, Cutaneous
0.700 1.000 1 2015 2015
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs2187668
rs2187668
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03
Autoimmune Hepatitis with Centrilobular Necrosis
0.700 1.000 1 2014 2014