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: rs3024490
rs3024490
0.846 0.250 1 206771966 intron variant A/C,G,T snp 0.69; 9.6E-05
CUI: C0042164
Disease: Uveitis
Uveitis
0.010 1.000 1 2010 2010
dbSNP: rs3024490
rs3024490
0.846 0.250 1 206771966 intron variant A/C,G,T snp 0.69; 9.6E-05
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.700 1 2013 2013
dbSNP: rs3024490
rs3024490
0.846 0.250 1 206771966 intron variant A/C,G,T snp 0.69; 9.6E-05
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 1.000 1 2015 2015
dbSNP: rs3024490
rs3024490
0.846 0.250 1 206771966 intron variant A/C,G,T snp 0.69; 9.6E-05
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic
0.010 1.000 1 2015 2015
dbSNP: rs3024500
rs3024500
1.000 0.071 1 206767486 intergenic variant A/C,G,T snp 0.42; 3.2E-05
CUI: C0024534
Disease: Malaria, Cerebral
Malaria, Cerebral
0.010 1.000 1 2013 2013
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.820 1.000 4 2010 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 1.000 3 2011 2013
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.030 1.000 3 2011 2013
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 1.000 2 2015 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 1.000 2 2015 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.020 1.000 2 2015 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.020 1.000 2 2011 2015
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
0.020 1.000 2 2015 2017
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 < 0.001 1 2011 2011
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2018 2018
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.010 1.000 1 2014 2014
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
0.010 < 0.001 1 2012 2012
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone
0.010 1.000 1 2017 2017
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0153382
Disease: Malignant neoplasm of oropharynx
Malignant neoplasm of oropharynx
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
0.010 < 0.001 1 2014 2014