Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
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
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs28937900 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4818 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs4633 0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs781565158 0.851 0.120 12 21452130 missense variant A/G snv 4.7E-05 2.1E-05 22
rs1555735545 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 22
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs2073618 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs1815739 0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17