Disease: Serum total cholesterol measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 8
rs56131196
APOC1
0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18 6
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 5
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv 4
rs12721109
APOC4 ; APOC4-APOC2
1.000 0.080 19 44943964 intron variant G/A snv 1.3E-02 3
rs769446
APOE
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 3
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 3