Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6
rs4711690
PGC
0.882 0.080 6 41741200 missense variant C/G snv 0.19 0.20 3
rs2301756 0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1130233 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs6939861 0.882 0.080 6 41735303 intron variant G/A snv 0.24 3
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs9315542 1.000 0.040 13 38057334 intron variant T/C snv 0.26 1
rs3781619 0.882 0.080 11 47233766 intron variant G/A snv 0.26 3
rs6498486 0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs6878265 1.000 0.040 5 120069960 intergenic variant C/T snv 0.29 2
rs8111742 0.851 0.120 19 51692221 intron variant G/A;C snv 0.30 4
rs3805246 0.882 0.120 4 143382955 intron variant G/A snv 0.31 3
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1886753 1.000 0.040 6 40359357 non coding transcript exon variant C/T snv 0.42 1
rs760805 0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs2607775
XPC ; LSM3
0.807 0.160 3 14178595 5 prime UTR variant C/G snv 0.42 0.43 8
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs2920283
JRK ; PSCA
0.925 0.040 8 142675619 intron variant T/C snv 0.44 2
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs7481521 1.000 0.040 11 1027811 missense variant C/T snv 0.50 0.47 1
rs6672420 0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50 6