Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs11613352 0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs769455 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8