Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs652438 0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1549758 0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7679 0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs2082940 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2259816 0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 8
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19