Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519705
KIT
1.000 0.040 4 54727464 missense variant A/G snv 1
rs1057519706
KIT
1.000 0.040 4 54727474 missense variant T/G snv 1
rs1057519708
KIT
1.000 0.040 4 54728096 missense variant T/A;G snv 2
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv 22
rs1057519713
KIT
0.925 0.120 4 54736498 missense variant G/C snv 3
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 2
rs1057519720
BRAF
0.851 0.080 7 140781602 missense variant CC/AA;GA mnv 4
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs1057519730
MAP2K1
1.000 0.040 15 66436786 missense variant T/A;G snv 2
rs1057519731
MAP2K1
0.925 0.040 15 66436816 missense variant G/C snv 2
rs1057519732
MAP2K1
0.827 0.160 15 66436824 missense variant C/A;T snv 6
rs1057519733
MAP2K1
1.000 0.040 15 66481793 missense variant G/A snv 1
rs1057519734
MAP2K1
1.000 0.040 15 66485086 missense variant C/T snv 1
rs1057519735
SNAPC5 ; MAP2K1
1.000 0.040 15 66490577 missense variant A/C snv 1
rs1057519742
GNA11
0.827 0.160 19 3118944 missense variant A/C;T snv 7
rs1057519804
AKT1
1.000 0.040 14 104776711 missense variant G/T snv 2
rs1057519805
MAP2K1
1.000 0.040 15 66436839 missense variant T/C snv 3
rs1057519806
MAP2K2
0.882 0.200 19 4110583 missense variant T/C snv 3
rs1057519807
MAP2K2
1.000 0.040 19 4110586 missense variant A/T snv 1
rs1057519808
MAP2K2
1.000 0.040 19 4117543 missense variant T/G snv 2
rs1057519809
MAP2K2
1.000 0.040 19 4117586 missense variant G/A;C snv 4.0E-06 1
rs1057519810
MAP2K2
1.000 0.040 19 4117619 missense variant C/A;T snv 4.0E-06 1
rs1057519811
PDGFRA
1.000 0.040 4 54274916 missense variant C/T snv 1
rs1057519812
PDGFRA
1.000 0.040 4 54277977 missense variant T/C snv 1