Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 267
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 70
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 60
rs121913254 0.647 0.429 1 114713909 missense variant G/A,C,T snp 33
rs121913364 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 25
rs11547328 0.715 0.357 12 57751648 missense variant G/A,T snp 4.0E-06 21
rs121913227 0.707 0.214 7 140753336 missense variant AC/CT,TT multinucleotide-polymorphism 16
rs121913512
KIT
0.846 0.107 4 54728055 missense variant A/C,G snp 8
rs3775292 0.821 0.071 4 186081871 non coding transcript exon variant C/G snp 0.84 6
rs723526 0.923 0.036 7 55067126 intron variant A/G snp 0.86 3
rs7668666 0.923 0.036 4 186080138 intron variant C/A,T snp 0.22; 3.2E-05 3
rs71310379 1.000 0.036 3 179199003 missense variant C/A snp 4.4E-05 3.2E-05 2