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
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs121917893 0.807 0.160 X 71167508 missense variant C/T snv 10
rs301430 0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs201551401 0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3
rs3747333 0.925 0.040 X 5893491 missense variant G/A;C;T snv 7.6E-03 3
rs3747334 0.925 0.040 X 5893489 synonymous variant G/A;C;T snv 1.2E-05; 6.7E-03 3
rs4141463 0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs768913131 0.925 0.040 2 50552821 missense variant G/A snv 3