Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs2023239 0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs806368 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs2609997 0.882 0.120 8 56447926 intron variant T/C snv 0.34 3
rs604300 1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs1019238 0.925 0.080 17 56201354 intron variant G/A;C snv 2
rs1431318 0.925 0.080 17 56115162 intron variant A/G snv 0.64 2
rs806380 0.925 0.120 6 88154934 intron variant A/G snv 0.26 2
rs2576573 0.925 0.120 8 56445416 3 prime UTR variant G/A snv 0.38 2
rs12491921 0.925 0.080 3 106570103 intergenic variant T/C snv 0.44 2
rs17664708 1.000 0.080 8 32579499 intron variant C/T snv 1.0E-01 2
rs7162140 1.000 0.080 15 34018399 5 prime UTR variant C/G;T snv 0.15 1