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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs2236418 0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6