Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 5
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs17410914 8 19985951 intergenic variant C/A;T snv 4
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 6
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 5
rs17411126 8 19997761 intergenic variant T/C snv 0.26 4
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs17489268 8 19994534 regulatory region variant T/A snv 0.25 4
rs17489282 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 4
rs1919484 1.000 0.040 8 20012165 intergenic variant G/A snv 0.23 4
rs1936800 6 127114919 intron variant C/T snv 0.51 4
rs2000571 11 116714817 regulatory region variant A/G snv 0.73 3
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 4
rs247615 16 56950851 regulatory region variant A/G snv 0.23 3
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7