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: rs1123339
rs1123339
17 49789170 non coding transcript exon variant G/A snv 6.6E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018
dbSNP: rs1123339
rs1123339
17 49789170 non coding transcript exon variant G/A snv 6.6E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs35388001
rs35388001
17 49779962 intron variant C/T snv 0.20
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs35388001
rs35388001
17 49779962 intron variant C/T snv 0.20
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs575705078
rs575705078
17 49779547 intron variant A/G snv 6.1E-04
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs79041579
rs79041579
17 49783553 intron variant G/A snv 0.15
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs79041579
rs79041579
17 49783553 intron variant G/A snv 0.15
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019