Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 32
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 39
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 45
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46