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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13