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: rs2777795
rs2777795
9 104910084 intron variant G/A snv 8.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2777795
rs2777795
9 104910084 intron variant G/A snv 8.8E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2777795
rs2777795
9 104910084 intron variant G/A snv 8.8E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012