Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 1
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 1
rs104894366
KRAS
0.776 0.400 12 25245284 missense variant G/A;C snv 2
rs1057519709
KIT
0.925 0.080 4 54733154 missense variant GA/AT mnv 1
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 1
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 1
rs111033563
LOC108783645 ; HFE
0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 1
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 1
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs1169288572
SETD2
1.000 0.040 3 47122237 missense variant C/T snv 8.0E-06 7.0E-06 1
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 1
rs121912472
INSL6 ; JAK2
0.925 0.080 9 5073742 missense variant G/C snv 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 1
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 1