Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.820 0.667 2 2011 2018
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 3 2011 2019
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.800 1.000 1 2011 2013
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.710 1.000 2 2013 2018
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs4129267
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019