Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121908585
PDGFRA
0.827 0.080 4 54285926 missense variant A/T snv 9
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G 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
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
rs121913516
KIT
1.000 0.080 4 54729353 missense variant C/T snv 4.0E-06 6
rs121913517
KIT
0.851 0.120 4 54727444 missense variant T/A;C;G snv 6
rs202101384
SDHB
0.851 0.160 1 17044818 missense variant T/A snv 4.4E-05 1.4E-05 6
rs1057519711
KIT
0.882 0.240 4 54733168 missense variant T/A snv 5
rs121908586
PDGFRA
1.000 0.080 4 54274869 missense variant T/A;C snv 5
rs138996609
SDHB
0.882 0.080 1 17022685 missense variant G/A snv 8.0E-06 7.0E-06 5
rs267607032
SDHB
0.882 0.080 1 17028605 missense variant C/A snv 1.2E-05 2.8E-05 5
rs587782243
SDHB
0.882 0.080 1 17033060 missense variant C/T snv 1.2E-05 7.0E-06 5
rs74315367
SDHB
0.882 0.080 1 17024025 missense variant G/C snv 4.0E-06 5
rs74315368
SDHB
0.882 0.080 1 17022648 missense variant C/T snv 1.2E-05 1.4E-05 5
rs786202732
SDHB
0.882 0.080 1 17024041 missense variant A/G snv 5
rs786203251
SDHB
0.882 0.080 1 17022649 missense variant G/A;T snv 5