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
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs769540300 0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs2236418 0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6
rs75012854 0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5
rs774847933 0.882 0.200 22 19962797 missense variant A/G snv 8.0E-06 5