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
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs6859 0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 6