Disease: Triglycerides measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs5112
APOC1P1
1.000 0.080 19 44927023 non coding transcript exon variant C/G snv 0.55 5
rs72836561
CD300LG
17 43848758 missense variant C/T snv 2.2E-02 2.0E-02 4