Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3735964
LPL
1.000 0.080 8 19966534 3 prime UTR variant C/A snv 9.1E-02 4
rs4149268 1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 4
rs481843 1.000 0.040 11 116655150 non coding transcript exon variant C/T snv 8.8E-02 4
rs6065904 1.000 0.080 20 45906012 intron variant G/A snv 0.23 4
rs6494005 1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 4
rs1059507
LPL
1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 3
rs12449157 1.000 0.040 16 67674994 3 prime UTR variant A/G snv 0.30 3
rs12686004 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 3
rs1461729 1.000 8 9329732 intron variant A/G snv 0.88 3
rs16940212 1.000 0.040 15 58401821 intron variant G/A;T snv 3
rs2271293 1.000 0.040 16 67868167 intron variant G/A snv 0.11 3
rs2281719 1.000 0.040 1 230161913 intron variant C/T snv 0.45 3
rs2338104 1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 3
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 3
rs2515629 1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs253
LPL
1.000 0.040 8 19953906 intron variant C/T snv 0.53 3
rs255049 1.000 0.040 16 67979568 intron variant T/C snv 0.34 3
rs263
LPL
1.000 0.040 8 19955301 intron variant C/T snv 0.23 3
rs271
LPL
1.000 0.040 8 19956191 intron variant G/A;T snv 3
rs285
LPL
1.000 0.080 8 19957678 intron variant C/T snv 0.59 3
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs3208305
LPL
1.000 0.080 8 19966137 3 prime UTR variant A/T snv 0.36 3
rs343
LPL
1.000 0.080 8 19953276 intron variant C/A snv 9.8E-02 8.1E-02 3
rs471364 1.000 0.040 9 15289580 intron variant C/T snv 0.87 3