Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs1057519742
GNA11
0.827 0.160 19 3118944 missense variant A/C;T snv 7
rs104894099
CDKN2A
0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06 5
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 5
rs993022333
KIT
0.851 0.080 4 54733173 missense variant A/C;T snv 5
rs4785763
AFG3L1P
0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv 3
rs121913337
BRAF
0.925 0.200 7 140753353 missense variant A/C;T snv 2
rs1990330
TEAD4
0.925 0.080 12 3038296 intron variant A/C;T snv 2
rs1057519703
KIT
1.000 0.040 4 54727418 missense variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 15
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs12628
LRRC56 ; HRAS
0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34 10
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 9
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs1799944
BRCA2
0.882 0.080 13 32337326 missense variant A/G snv 5.4E-02 4.5E-02 5
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv 4