Disease: Serum total cholesterol measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 3
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs2980875 8 125469505 intron variant A/C;G;T snv 4
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 3
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 3
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 2
rs12721054
APOC1
19 44919330 3 prime UTR variant A/G snv 3.7E-02 3
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 4
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13