Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs549543886 8 11759643 3 prime UTR variant T/C snv 2.2E-03 1
rs546772104 6 139373448 missense variant G/A;T snv 5.0E-06; 5.0E-06 1
rs10503425 8 11748855 intron variant G/A;C snv 1
rs113049875 8 11755236 intron variant G/A;C;T snv 1
rs116052854 8 11757212 intron variant C/A;T snv 1
rs12156163 8 11757260 intron variant C/G;T snv 1
rs147860174 8 11750261 intron variant G/A snv 5.3E-03 5.4E-03 1
rs1554498312 8 11754991 intron variant T/C snv 1
rs1554498708 8 11756909 non coding transcript exon variant G/A snv 1
rs3729851 8 11755333 intron variant G/A snv 9.3E-02 1
rs3735819 8 11748803 intron variant T/C snv 0.80 1
rs745379 8 11758186 intron variant A/G snv 0.39 1
rs773626580 8 11758384 missense variant C/T snv 1.2E-05 7.0E-06 1
rs864321698 8 11708335 missense variant C/A;T snv 1
rs864321700 8 11708695 missense variant A/T snv 1
rs864321701 8 11708709 missense variant A/T snv 1
rs864321702 8 11748984 missense variant T/A snv 1
rs864321703 8 11708339 missense variant C/A snv 1
rs864321704 8 11758409 synonymous variant C/T snv 1
rs864321705 8 11755135 splice donor variant T/G snv 1
rs804290 8 11759327 3 prime UTR variant G/A;C snv 1
rs145570263 9 100292626 missense variant C/A;T snv 4.0E-06 1
rs751426149 14 23389617 stop gained G/A;T snv 4.0E-06; 4.0E-06 1
rs760414580 17 12744241 missense variant A/G snv 1.0E-04 1.4E-05 1
rs864321645 5 173233210 splice acceptor variant C/A snv 1