Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45 3
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1036935 0.925 0.120 18 50317164 upstream gene variant A/G;T snv 2
rs1041569
TNFSF13B
1.000 0.120 13 108267195 intron variant T/A;C snv 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1044873
IRF8
0.925 0.120 16 85922065 3 prime UTR variant C/T snv 0.40 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 4
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 7
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 7
rs1057519831
PLCG2
1.000 0.120 16 81912655 missense variant C/T snv 3
rs1057519832
PLCG2
1.000 0.120 16 81928578 missense variant A/C;G;T snv 1
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519959
SF3B2
0.882 0.200 11 66063028 missense variant A/C snv 4
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs1057519961
SF3B1
0.851 0.240 2 197402759 missense variant C/T snv 4