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: rs1042034
rs1042034
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2010 2019
dbSNP: rs1042034
rs1042034
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
High density lipoprotein measurement
0.800 1.000 4 2010 2019
dbSNP: rs1042034
rs1042034
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs1042034
rs1042034
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs1042034
rs1042034
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs1042034
rs1042034
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
Red cell distribution width determination
0.700 1.000 1 2019 2019