Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554290 0.618 0.464 1 114713908 missense variant T/A,C,G snp 9
rs121913503 0.724 0.179 15 90088606 missense variant C/A,T snp 7
rs121913237 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 6
rs267607040 0.846 0.286 18 44951948 missense variant G/A snp 6
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 5
rs121918453 0.756 0.286 12 112450394 missense variant G/A,C,T snp 5
rs121918454 0.756 0.286 12 112450395 missense variant C/A,G,T snp 5
rs77375493 0.504 0.536 9 5073770 missense variant G/A,T snp 3.5E-04 2.9E-04 4
rs112445441 0.699 0.286 12 25245347 missense variant snp 4
rs121434595 0.692 0.357 1 114716124 missense variant C/A,G,T snp 4
rs121913254 0.647 0.429 1 114713909 missense variant G/A,C,T snp 4
rs104894228 0.662 0.500 11 534286 missense variant C/A,G,T snp 3
rs104894230 0.615 0.464 11 534288 missense variant C/A,G,T snp 3
rs121913506
KIT
0.692 0.286 4 54733154 missense variant G/A,C,T snp 3
rs121434596 0.707 0.357 1 114716123 missense variant C/A,G,T snp 4.0E-06; 4.0E-06 3
rs121918460 0.756 0.214 12 112450364 stop lost T/A,G snp 4.0E-06 3
rs121912666 0.647 0.321 17 7674872 missense variant T/C,G snp 8.0E-06 3
rs28931590 1.000 0.036 19 33302164 missense variant T/A snp 2
rs121913487 0.923 0.107 13 28018503 stop gained A/C,T snp 2
rs387906631 0.923 0.071 3 128481901 missense variant G/A snp 2
rs111033563 0.801 0.214 6 26092916 missense variant A/C snp 4.0E-06 2
rs104894226 0.692 0.464 11 534285 missense variant C/A,G,T snp 2
rs104894229 0.634 0.500 11 534289 missense variant C/A,G,T snp 2
rs121917759 0.801 0.321 11 533466 missense variant G/A snp 2
rs121913499 0.630 0.464 2 208248389 missense variant G/A,C,T snp 2