rs11168249, HDAC7

N. diseases: 9
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 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.800 1.000 1 2012 2012
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 3 2015 2017
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 2 2013 2016
Primary sclerosing cholangitis
CUI: C0566602
Disease: Primary sclerosing cholangitis
58 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 2 2011 2013
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 1 2016 2016
Lymphocyte Count measurement
CUI: C0200635
Disease: Lymphocyte Count measurement
456 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 1 2016 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 1 2019 2019