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: rs1015538
rs1015538
7 100028412 intron variant A/G snv 0.72
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs142529006
rs142529006
7 100022093 intron variant T/A snv 6.9E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
7 100022093 intron variant T/A snv 6.9E-03
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
7 100022093 intron variant T/A snv 6.9E-03
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
7 100022093 intron variant T/A snv 6.9E-03
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs1963304
rs1963304
7 100028173 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2897075
rs2897075
1.000 0.040 7 100032719 intron variant C/T snv 0.31
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.700 1.000 1 2019 2019