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: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2017 2017
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 1.000 1 2018 2018
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
0.010 1.000 1 2018 2018
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2019 2019
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0040561
Disease: Ocular Toxoplasmosis
Ocular Toxoplasmosis
0.010 1.000 1 2018 2018
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.010 1.000 1 2018 2018
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.010 1.000 1 2019 2019
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis
0.010 1.000 1 2019 2019
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2012 2012
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2015 2015
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
Classical Hodgkin's Lymphoma
0.010 1.000 1 2013 2013
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.010 1.000 1 2016 2016
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2010 2010
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C4290046
Disease: trachomatis
trachomatis
0.010 1.000 1 2015 2015
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
Tuberculosis, extrapulmonary
0.010 1.000 1 2019 2019
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C1304470
Disease: Generalized vitiligo
Generalized vitiligo
0.010 1.000 1 2013 2013
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0038443
Disease: Stress, Psychological
Stress, Psychological
0.010 1.000 1 2015 2015
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2015 2015
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0026918
Disease: Mycobacterium Infections
Mycobacterium Infections
0.010 1.000 1 2014 2014
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura
0.010 1.000 1 2014 2014
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0006060
Disease: Boutonneuse Fever
Boutonneuse Fever
0.010 1.000 1 2009 2009
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 1.000 1 2014 2014
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C4025886
Disease: Severe periodontitis
Severe periodontitis
0.010 1.000 1 2019 2019
dbSNP: rs2430561
rs2430561
0.590 0.760 12 68158742 intron variant T/A snv 0.36
CUI: C0038522
Disease: Subacute Sclerosing Panencephalitis
Subacute Sclerosing Panencephalitis
0.010 1.000 1 2007 2007