Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10255208 0.925 0.160 7 36819038 non coding transcript exon variant A/G snv 0.46 2
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1063537 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10823108 0.925 0.160 10 67900736 intron variant G/A snv 7.1E-02 2
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137933 0.882 0.160 17 27778906 synonymous variant G/A snv 0.20 0.21 4
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11643718 0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 10
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs11771443 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs117897666 0.882 0.160 15 73811619 intergenic variant C/T snv 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs136161 0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs1411766 0.882 0.160 13 109599813 intron variant G/A;T snv 3
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs143101792
CRP
0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 5
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1531343 0.925 0.160 12 65781114 intron variant G/C;T snv 2
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36