Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10246939 0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 6
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2307111 0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1805096 0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 6
rs17848939 1.000 0.080 17 82085473 intron variant C/G;T snv 5.0E-06; 0.45 1
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5574 0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 5
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs12218 0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs3748024 0.925 0.080 2 112588836 3 prime UTR variant C/G snv 0.41 0.35 3
rs4215 1.000 0.080 7 99971771 missense variant G/A;C snv 0.41 1
rs225014 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs1799722 0.882 0.240 14 96204802 5 prime UTR variant C/T snv 0.41 0.39 4
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2229765 0.807 0.280 15 98934996 synonymous variant G/A snv 0.40 0.39 7
rs12199580 1.000 0.080 6 36302353 missense variant C/A;T snv 0.40 1
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs11545881 0.925 0.080 18 12274105 missense variant G/A;C;T snv 1.2E-05; 0.37 2
rs180743 1.000 0.080 16 28496323 missense variant C/G snv 0.36 0.40 1
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106