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.
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
14 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2009 2009
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2016 2016
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2016 2016
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
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2013 2013
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2013 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.641 0.600 6 31572536 intron variant A/G;T snv 0.700 0
PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO (finding)
1 0.641 0.600 6 31572536 intron variant A/G;T snv 0.700 0