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: rs4759375
rs4759375
12 123311691 intron variant C/T snv 7.8E-02
High density lipoprotein measurement
0.800 1.000 2 2010 2019
dbSNP: rs4759375
rs4759375
12 123311691 intron variant C/T snv 7.8E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013