Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv 22
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 16
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs4149117
SLCO1B3-SLCO1B7 ; SLCO1B3
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 14
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs2230774
ROCK2
0.807 0.240 2 11218994 missense variant G/C;T snv 0.49 12
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 9
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs1052667
ARHGAP35
0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs730882002
TP53
0.925 0.040 17 7674956 missense variant T/C snv 6
rs768827923
PIK3CD
0.851 0.080 1 9721816 missense variant T/G snv 6
rs771386507
HLA-B ; MIR6891
0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs1490204625
RASA1
0.925 0.160 5 87268486 missense variant G/A snv 5
rs2064863
AURKA
0.925 0.120 20 56387716 intron variant T/A;C;G snv 4
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4