Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1555640521 0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs301430 0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7