Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2695165 15 41781199 intron variant C/T snv 1.00 0.42 1
rs4758675 12 122207191 missense variant C/A;G snv 1.00 0.99 1
rs2797436 0.925 0.040 1 237700418 synonymous variant T/A;G snv 7.0E-05; 0.99 2
rs6670122 0.882 0.120 1 156737983 intron variant T/C;G snv 0.99 2
rs614754 6 160084167 synonymous variant C/G snv 0.99 0.99 1
rs690346 1.000 0.080 15 53716648 missense variant T/C snv 0.99 0.96 1
rs6736913 1.000 0.040 2 42282878 stop gained A/G;T snv 0.99 1
rs4387351 1.000 0.040 11 62613260 5 prime UTR variant T/C snv 0.98 0.94 2
rs105633 0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs6050446 20 25214873 stop gained A/G;T snv 0.98 1
rs1144566 1 182600491 missense variant T/A;C;G snv 0.98 1
rs2664521 20 48636612 stop gained T/A;C snv 0.98 1
rs1013579
C8B
1 56956811 missense variant C/T snv 0.98 0.98 1
rs1435547 1.000 0.080 2 11597965 missense variant T/A;C snv 0.98 1
rs3744644 1.000 0.080 17 1635334 missense variant C/A;G snv 1.6E-05; 0.97 1
rs428113 1.000 0.040 19 2991816 intron variant T/A;C;G snv 0.97; 4.0E-06 1
rs6472812 1.000 0.080 8 74004849 missense variant A/G snv 0.97 0.97 1
rs12147030 1.000 0.040 14 89401634 missense variant T/C snv 0.97 0.93 1
rs7105056 11 112193708 non coding transcript exon variant T/C snv 0.97 0.95 1
rs643507 1.000 0.080 18 2946293 non coding transcript exon variant C/T snv 0.96 0.92 1
rs908830 9 136946407 intron variant T/C snv 0.96 0.95 1
rs10283100 8 119583783 missense variant A/G;T snv 0.96 3
rs299163 19 55810048 missense variant C/A;T snv 0.96 1
rs758386 3 45775926 stop gained A/G;T snv 0.96 1
rs6784615 1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1