Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs878886 0.925 0.080 17 45835124 3 prime UTR variant C/G;T snv 2
rs1396862 1.000 0.040 17 45825631 non coding transcript exon variant G/A snv 0.14 2
rs16940674 1.000 0.040 17 45833141 missense variant C/T snv 0.15 0.14 2
rs1876829 1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs1912151 1.000 0.040 17 45825578 splice region variant C/T snv 0.25 0.14 2
rs4640231 1.000 0.040 17 45835420 3 prime UTR variant G/A;C snv 0.14 2
rs17763086 1.000 0.040 17 45828115 intron variant T/G snv 0.14 2
rs878887 1.000 0.040 17 45835216 3 prime UTR variant C/T snv 0.14 2
rs16940665 1.000 0.040 17 45830530 stop lost T/C snv 0.15 0.14 2
rs1876828 0.851 0.160 17 45834159 intron variant C/T snv 0.14 1
rs4525537 1.000 0.040 17 45835357 3 prime UTR variant T/C snv 0.14 1
rs16940668 1.000 0.040 17 45830600 non coding transcript exon variant G/A snv 0.15 0.14 1
rs16940677 1.000 0.040 17 45834532 intron variant C/T snv 0.14 1
rs17425752 1.000 0.040 17 45829360 splice region variant A/C snv 0.15 0.14 1
rs1876830 1.000 0.040 17 45833986 intron variant C/T snv 0.15 0.14 1
rs4482334 1.000 0.040 17 45835464 3 prime UTR variant T/C snv 0.14 1
rs878888 1.000 0.040 17 45835269 3 prime UTR variant A/G snv 0.14 1
rs12150390 1.000 0.040 17 45818862 intron variant T/C snv 0.14 1
rs16940676 1.000 0.040 17 45833670 intron variant G/A snv 0.14 0.14 1
rs2316765 1.000 0.040 17 45835088 3 prime UTR variant T/C snv 0.14 1