Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs115160714
TOPBP1
0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
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
rs6024836
FAM210B ; AURKA
0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 7
rs1052667
ARHGAP35
0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs11902171
ITGAV
0.925 0.080 2 186678500 3 prime UTR variant G/C snv 0.22 6
rs60745952
LOC107986195 ; LOC105377481
0.925 0.080 4 148827842 intron variant T/C snv 0.13 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
rs10817938
PTCSC2
0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
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
rs1040411
ATG5
1.000 0.120 6 106150148 intron variant G/A snv 0.47 3
rs12881063
LOC107984671 ; LOC105370397
1.000 0.080 14 20788017 downstream gene variant G/C snv 7.4E-02 3
rs1340026226
AR
1.000 0.080 X 67711662 missense variant G/A snv 9.5E-06 3
rs200081710
TNIP3
1.000 0.120 4 121154648 missense variant T/C snv 7.0E-06 3
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3