Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs11538209
ALB
1.000 0.120 4 73404356 missense variant T/C snv 2
rs58624704
ALB
0.925 0.200 4 73410325 missense variant G/A snv 8.0E-06 3.5E-05 2
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs136161 0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs3807337 1.000 0.120 7 134779071 intron variant A/G;T snv 1
rs3917887 0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33 8
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1532624 0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs4783961 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 7
rs39075 1.000 0.120 7 29237076 intron variant G/A snv 0.41 1
rs805304 0.851 0.240 6 31730311 5 prime UTR variant T/G snv 0.48 5
rs2346061 1.000 0.120 18 74533297 upstream gene variant C/A snv 0.71 1
rs7577 1.000 0.120 18 74521112 3 prime UTR variant T/A;C;G snv 0.21 1
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs3742264 0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs1926447 0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs143101792
CRP
0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 5
rs762285755 0.925 0.160 10 17114074 missense variant T/C snv 7.6E-05 2.8E-05 2
rs1252906 1.000 0.120 14 59192073 intron variant A/C;G snv 1
rs994411260 0.925 0.160 19 10194877 missense variant G/C snv 2