rs2227284, IL4

N. diseases: 12
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.
Asthma
CUI: C0004096
Disease: Asthma
1536 0.732 0.480 5 132677033 intron variant T/C;G snv 0.030 1.000 3 2013 2015
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.732 0.480 5 132677033 intron variant T/C;G snv 0.020 1.000 2 2013 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1 2019 2019
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2017 2017
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2004 2004
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2013 2013
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1 2019 2019
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2010 2010
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1 2019 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2010 2010
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2017 2017
Rhinoconjunctivitis
CUI: C0861155
Disease: Rhinoconjunctivitis
16 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2012 2012