rs13277237, CCDC26

N. diseases: 4
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.
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 8 129592317 intron variant G/A snv 0.53 0.700 1.000 1 2019 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 8 129592317 intron variant G/A snv 0.53 0.700 1.000 1 2015 2015
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 8 129592317 intron variant G/A snv 0.53 0.700 1.000 1 2017 2017
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 8 129592317 intron variant G/A snv 0.53 0.700 1.000 1 2017 2017