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: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs145922845
rs145922845
1.000 0.040 1 206772393 missense variant C/T snv 1.9E-03 1.8E-03
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.030 0.667 3 2000 2005
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.030 1.000 3 2007 2016
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.020 1.000 2 2007 2016
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 1.000 2 2007 2015
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 1.000 2 2007 2011
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2007 2007
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.010 1.000 1 2007 2007
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.010 1.000 1 2007 2007
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.030 1.000 3 2008 2016
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.030 1.000 3 2008 2016
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.020 1.000 2 2008 2016
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.020 1.000 2 2008 2016
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
0.010 1.000 1 2008 2008
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0079745
Disease: Lymphoma, Large-Cell, Follicular
Lymphoma, Large-Cell, Follicular
0.010 1.000 1 2008 2008
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 1.000 1 2008 2008
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 0.750 4 2009 2014
dbSNP: rs3024493
rs3024493
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 1.000 3 2009 2016
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.020 1.000 2 2009 2016