rs4149576, TNFRSF1A

N. diseases: 3
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.
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.882 0.200 12 6339949 intron variant C/T snv 0.32 0.700 1.000 1 2009 2009
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.882 0.200 12 6339949 intron variant C/T snv 0.32 0.700 1.000 1 2017 2017
Paranoid Schizophrenia
CUI: C0036349
Disease: Paranoid Schizophrenia
23 0.882 0.200 12 6339949 intron variant C/T snv 0.32 0.010 1.000 1 2017 2017