rs6840978, IL21-AS1

N. diseases: 10
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.
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.800 1.000 2 2011 2019
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.710 1.000 3 2007 2015
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
116 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.700 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.020 1.000 2 2009 2009
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.010 1.000 1 2010 2010
Primary sclerosing cholangitis
CUI: C0566602
Disease: Primary sclerosing cholangitis
58 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.010 1.000 1 2011 2011
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.010 1.000 1 2010 2010