rs4845604, RORC

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.
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.800 1.000 3 2012 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 3 2015 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 3 2015 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
Eczema
CUI: C0013595
Disease: Eczema
368 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
Respiratory Tract Diseases
CUI: C0035242
Disease: Respiratory Tract Diseases
109 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019