Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs12953717 0.724 0.240 18 48927559 intron variant C/T snv 0.36 18