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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs1805127 0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs2682826 0.807 0.280 12 117215033 3 prime UTR variant G/A snv 0.25 11
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs2288904 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs41279104 0.827 0.160 12 117439680 intron variant C/T snv 0.11 6
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 5
rs2075575 0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
rs11096955 0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41 5