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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
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
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18