Disease: Triglycerides measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs1713222 2 21048451 upstream gene variant A/G snv 0.82 3
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2523575 6 31361049 upstream gene variant C/G snv 0.20 4
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs563290 2 21065354 intergenic variant G/A snv 0.69 4
rs585362 1 109247173 upstream gene variant C/G;T snv 4