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: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2017 2017
dbSNP: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2017 2017