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: rs11789603
rs11789603
9 104884738 intron variant C/T snv 0.11
High density lipoprotein measurement
0.800 1.000 1 2012 2018
dbSNP: rs11789603
rs11789603
9 104884738 intron variant C/T snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012