Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6498486 0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs7749023 1.000 0.040 6 42093995 non coding transcript exon variant A/C;T snv 1
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2301756 0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs158916 0.882 0.080 5 60949318 intron variant A/G snv 0.15 3
rs3814896 0.882 0.080 21 42351602 upstream gene variant A/G snv 0.17 3
rs2014486 1.000 0.040 11 1237573 intron variant A/G snv 0.52 2
rs7747696 1.000 0.040 6 42093217 non coding transcript exon variant A/G snv 0.54 1
rs760805 0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs6672420 0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50 6
rs629367 0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs11536878 0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs121434254 0.807 0.200 21 44289773 stop gained C/A;T snv 7.5E-04 6
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2607775
XPC ; LSM3
0.807 0.160 3 14178595 5 prime UTR variant C/G snv 0.42 0.43 8
rs4711690
PGC
0.882 0.080 6 41741200 missense variant C/G snv 0.19 0.20 3
rs3789210
PGC
0.882 0.080 6 41743584 intron variant C/G;T snv 3
rs765803011 1.000 0.040 16 27363094 missense variant C/G;T snv 4.0E-06; 1.6E-05 1
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs1130233 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13