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: rs10267576
rs10267576
7 44831334 intron variant T/C snv 0.35
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs12155038
rs12155038
7 44833378 intron variant G/A snv 0.40
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12155039
rs12155039
7 44833526 intron variant C/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs12155039
rs12155039
7 44833526 intron variant C/A;T snv
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs7789162
rs7789162
7 44833301 intron variant T/C snv 0.48
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs7789162
rs7789162
7 44833301 intron variant T/C snv 0.48
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs7789162
rs7789162
7 44833301 intron variant T/C snv 0.48
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019