Source: GWASDB

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: rs605066
rs605066
6 139508529 intron variant C/T snv 0.53
High density lipoprotein measurement
0.800 1.000 2 2010 2019
dbSNP: rs605066
rs605066
6 139508529 intron variant C/T snv 0.53
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013
dbSNP: rs605066
rs605066
6 139508529 intron variant C/T snv 0.53
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs605066
rs605066
6 139508529 intron variant C/T snv 0.53
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012