Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 4
rs1057520031
KIT
1.000 0.040 4 54727440 missense variant A/C;G snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs993022333
KIT
0.851 0.080 4 54733173 missense variant A/C;T snv 3
rs1312268347
SARDH
0.925 0.120 9 133734172 start lost A/G snv 5.0E-06 4
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 51
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
rs121908585
PDGFRA
0.827 0.080 4 54285926 missense variant A/T snv 9
rs1057519700
PDGFRA
4 54277981 missense variant C/A;G snv 1
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 5
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 3
rs371828253
CUX1
7 102273431 missense variant C/G snv 2.4E-05 4.2E-05 1
rs1285675735
SORD
0.827 0.200 15 45043384 synonymous variant C/G;T snv 1.1E-05; 1.1E-05 6
rs397516835
SDHB
0.925 0.080 1 17024040 missense variant C/G;T snv 1
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 23
rs121913516
KIT
1.000 0.080 4 54729353 missense variant C/T snv 4.0E-06 6
rs148634289
SDHD
0.827 0.200 11 112088925 synonymous variant C/T snv 1.6E-05 2.1E-05 6
rs764575966
SDHC
0.882 0.080 1 161356832 stop gained C/T snv 3.6E-05 7.0E-06 4
rs778015444
PDGFRA
1.000 0.040 4 54274917 missense variant C/T snv 4.0E-06 7.0E-06 2
rs1186206565
PECAM1
17 64352432 missense variant C/T snv 1
rs200871174
MSLN ; MIR662
16 768475 missense variant C/T snv 7.8E-04 3.6E-04 1