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: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 2 2016 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.700 1.000 2 2019 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0001925
Disease: Albuminuria
Albuminuria 		0.700 1.000 1 2018 2018
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		0.700 1.000 1 2019 2019
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs28601761
rs28601761 		1.000 0.040 8 125487789 intron variant C/G snv 0.37
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019