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: rs4362077
rs4362077
10 99828664 intron variant C/T snv 1.6E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs4362077
rs4362077
10 99828664 intron variant C/T snv 1.6E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012