Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Bronchitis
CUI: C0006277
Disease: Bronchitis
4 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.641 0.600 6 31572536 intron variant A/G;T snv 0.020 1.000 2 2012 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.641 0.600 6 31572536 intron variant A/G;T snv 0.020 1.000 2 2015 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.641 0.600 6 31572536 intron variant A/G;T snv 0.020 1.000 2 2012 2018
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.641 0.600 6 31572536 intron variant A/G;T snv 0.020 0.500 2 2006 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.641 0.600 6 31572536 intron variant A/G;T snv 0.020 1.000 2 2015 2019
Acquired Immunodeficiency Syndrome
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
42 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2019 2019
Temporomandibular Joint Disorders
CUI: C0039494
Disease: Temporomandibular Joint Disorders
25 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2019 2019