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: rs12052715
rs12052715
2 159820864 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2018 2018
dbSNP: rs12052715
rs12052715
2 159820864 intron variant C/G;T snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs12469306
rs12469306
2 159848974 intron variant A/G snv 0.87
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs12692572
rs12692572
2 159887282 intron variant G/A snv 0.41
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2018 2018
dbSNP: rs2556094
rs2556094
2 159829018 intron variant A/G snv 0.80
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2556097
rs2556097
2 159830550 intron variant C/A;T snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs2556097
rs2556097
2 159830550 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: rs41265133
rs41265133
2 159842189 intron variant A/C snv 0.63
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs78685880
rs78685880
2 159850033 missense variant A/G snv 2.3E-03 8.2E-04
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2018 2018