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: rs4791641
rs4791641
17 8257831 missense variant C/T snv 0.43 0.41
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2016 2017
dbSNP: rs4791641
rs4791641
17 8257831 missense variant C/T snv 0.43 0.41
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs4791641
rs4791641
17 8257831 missense variant C/T snv 0.43 0.41
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs4791641
rs4791641
17 8257831 missense variant C/T snv 0.43 0.41
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016