Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv 24
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv 22
rs1057519865
FOXL2NB ; FOXL2
0.742 0.240 3 138946321 missense variant G/C snv 15
rs4474514
KITLG
0.827 0.240 12 88560182 intron variant G/A snv 0.65 6
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 5
rs210138
GGNBP1 ; BAK1
0.851 0.240 6 33574761 intron variant A/G snv 0.19 5
rs746899020
TNFRSF1A
0.882 0.160 12 6329495 missense variant G/A;C snv 4.6E-06 3
rs4324715 0.925 0.160 5 142289942 regulatory region variant C/T snv 0.41 2
rs748835289
CASP8
0.925 0.160 2 201285037 missense variant G/T snv 4.0E-06 2
rs200292857
TNFRSF1A
0.925 0.160 12 6329974 synonymous variant G/A;C snv 4.8E-05 2
rs948662
GAB2
1.000 0.120 11 78268783 intron variant A/G snv 0.20 1