Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 1
rs387907097
TGM6
0.925 0.120 20 2417445 missense variant T/G snv 1.5E-04 5.6E-05 1
rs267606708
CBL
0.925 0.040 11 119278541 missense variant G/A snv 4.0E-06 2.1E-05 1
rs754921650
SETD2
1.000 0.040 3 47120446 missense variant T/C snv 1.2E-05 2.1E-05 1
rs1169288572
SETD2
1.000 0.040 3 47122237 missense variant C/T snv 8.0E-06 7.0E-06 1
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs267607040
SETBP1
0.851 0.320 18 44951948 missense variant G/A snv 4
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs104894366
KRAS
0.776 0.400 12 25245284 missense variant G/A;C snv 2
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
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
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv 2
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 2
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 2
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 2
rs387906631
GATA2
0.882 0.080 3 128481901 missense variant G/A snv 2