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: rs12480732
rs12480732
NOL4L-DT
20 32603213 intron variant C/T snv 0.19
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12480732
rs12480732
NOL4L-DT
20 32603213 intron variant C/T snv 0.19
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs6119267
rs6119267
NOL4L ; NOL4L-DT
20 32576112 intron variant C/A;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs6119267
rs6119267
NOL4L ; NOL4L-DT
20 32576112 intron variant C/A;G snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs6119267
rs6119267
NOL4L ; NOL4L-DT
20 32576112 intron variant C/A;G snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs67696533
rs67696533
NOL4L ; NOL4L-DT
20 32585560 intron variant G/A;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs7266642
rs7266642
NOL4L-DT
20 32593666 intron variant A/G snv 0.50
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019