rs1143633, IL1B

N. diseases: 10
Source: BEFREE ×
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.
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
178 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2007 2007
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
74 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
769 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
603 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
193 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2012 2012
Post-Traumatic Stress Disorder
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
101 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Restless Legs Syndrome
CUI: C0035258
Disease: Restless Legs Syndrome
44 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
1332 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2011 2011
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2012 2012
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
616 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2018 2018