Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs138450474 1.000 0.040 19 35039140 missense variant G/A;C snv 2.0E-05 1
rs143166100 1.000 0.040 9 128607988 missense variant C/G snv 5.7E-04 5.4E-04 1
rs1439688451 1.000 0.040 16 9798433 missense variant C/G;T snv 4.0E-06 1
rs1441152520 1.000 0.040 9 128632218 missense variant A/G snv 1
rs145873257 1.000 0.040 16 7709117 missense variant G/A;T snv 1.8E-03 1
rs147896487 1.000 0.040 8 18084767 missense variant C/G snv 1.3E-03 1.5E-03 1
rs150586939 1.000 0.040 18 47156119 splice region variant A/G snv 4.1E-03 1
rs150821246 1.000 0.040 8 132129618 missense variant C/T snv 3.7E-04 3.1E-04 1
rs1553138299 1.000 0.040 1 43403254 missense variant C/G snv 1
rs1553154643 1.000 0.040 1 43443774 missense variant C/T snv 1
rs1553155982 1.000 0.040 1 42928996 missense variant T/A snv 1
rs1553574522 1.000 0.040 2 165331362 missense variant T/C snv 1
rs1554098235 1.000 0.040 5 162104026 missense variant G/A snv 1
rs1554263366 1.000 0.040 6 145686284 missense variant T/C snv 1
rs1554626549 1.000 0.040 8 132170427 missense variant G/A snv 1
rs1554759745 1.000 0.040 9 128611792 missense variant G/A snv 1
rs1554770659 1.000 0.040 9 137163819 missense variant T/C snv 1
rs1555437424 1.000 0.040 15 92924407 missense variant G/A snv 1
rs1555445693 1.000 0.040 15 93014832 missense variant C/T snv 1
rs1555699052 1.000 0.040 17 63710782 missense variant C/T snv 1
rs1555790846 1.000 0.040 20 8790220 missense variant C/T snv 1
rs1555841977 1.000 0.040 21 6116503 missense variant C/T snv 1
rs180922748 1.000 0.040 2 166233432 missense variant G/C snv 1.2E-03 1.7E-03 1
rs187334123 1.000 0.040 22 31797646 missense variant G/A;T snv 2.2E-03; 1.6E-05 1
rs191333060 1.000 0.040 X 100296405 missense variant G/A;C snv 1.3E-03 1