Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10042590 5 88477501 intron variant G/A snv 5.8E-02 1
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs1008805 0.851 0.160 15 51257402 intron variant G/A snv 0.64 7
rs1009358 1.000 0.080 2 65049318 intron variant T/C snv 0.40 2
rs10107066 8 26542619 intron variant G/C snv 0.29 1
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs1030431 8 58399138 intergenic variant A/G;T snv 3
rs10306135 9 122375416 5 prime UTR variant A/T snv 0.14 1
rs10409243 19 10222312 3 prime UTR variant C/A;G;T snv 6
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042034 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs1042309696
ACE
17 63487006 synonymous variant T/C snv 2
rs1042580 20 23046984 3 prime UTR variant T/C snv 0.33 2
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1044486 17 78796097 3 prime UTR variant G/A snv 0.41 1
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1047964 11 117286177 3 prime UTR variant G/A;C;T snv 3
rs1048070 9 14735055 3 prime UTR variant T/C snv 0.46 1
rs10500326 16 4868325 intron variant G/T snv 0.21 1