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: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
Malignant neoplasm of colon and/or rectum
0.020 1.000 2 2009 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.010 1.000 1 2009 2009
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2009 2009
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.010 1.000 1 2009 2009
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0006060
Disease: Boutonneuse Fever
Boutonneuse Fever
0.010 1.000 1 2009 2009
dbSNP: rs2222202
rs2222202
0.827 0.160 1 206772036 intron variant G/A snv 0.39
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.010 1.000 1 2009 2009
dbSNP: rs3024496
rs3024496
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2009 2009
dbSNP: rs3024496
rs3024496
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.830 0.800 5 2010 2017
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
Diabetes Mellitus, Non-Insulin-Dependent
0.050 1.000 5 2010 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.050 0.800 5 2010 2020
dbSNP: rs1518111
rs1518111
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.830 1.000 4 2010 2015
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2010 2014
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 1.000 2 2010 2013
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.020 1.000 2 2010 2015
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
Diabetes Mellitus, Non-Insulin-Dependent
0.020 1.000 2 2010 2014
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0243026
Disease: Sepsis
Sepsis
0.020 1.000 2 2010 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0036690
Disease: Septicemia
Septicemia
0.020 1.000 2 2010 2016
dbSNP: rs1554286
rs1554286
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0014541
Disease: Epiglottitis
Epiglottitis
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0079745
Disease: Lymphoma, Large-Cell, Follicular
Lymphoma, Large-Cell, Follicular
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C2349952
Disease: Oropharyngeal Carcinoma
Oropharyngeal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.010 1.000 1 2010 2010
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2010 2010