rs1800890, IL19

N. diseases: 29
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.
Rhinovirus infection
CUI: C0276447
Disease: Rhinovirus infection
4 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.010 1.000 1 2018 2018
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.010 1.000 1 2018 2018
Waldenstrom Macroglobulinemia
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
15 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.010 1.000 1 2009 2009
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.010 1.000 1 2017 2017