Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108