Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48