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: rs1126930
rs1126930
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2016 2019
dbSNP: rs1126930
rs1126930
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs1126930
rs1126930
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs1126930
rs1126930
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs1126930
rs1126930
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs2117029
rs2117029
12 49014657 intron variant A/T snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2019 2019
dbSNP: rs2293445
rs2293445
12 49005079 intron variant G/A snv 0.37 0.36
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018