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
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
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
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs121913513
KIT
0.776 0.120 4 54727495 missense variant T/C snv 10
rs917411291
GZMM
0.851 0.360 19 544072 start lost A/C;G snv 9
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 9
rs121908585
PDGFRA
0.827 0.080 4 54285926 missense variant A/T snv 9
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 9
rs10509681
CYP2C8
0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 8
rs587782703
SDHB
0.807 0.160 1 17053947 splice donor variant C/A;T snv 1.2E-05; 4.1E-06 8
rs764575966
SDHC
0.882 0.080 1 161356832 stop gained C/T snv 3.6E-05 7.0E-06 8
rs587782604
SDHB
0.827 0.120 1 17022684 missense variant C/A;T snv 4.0E-06; 4.0E-06 7
rs786201095
SDHB
0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 7