Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 1
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs371246226
U2AF1
0.827 0.160 21 43094667 missense variant T/C;G snv 2.4E-05; 2.4E-05 1
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 1
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 1
rs377577594
DNMT3A
0.827 0.240 2 25234374 missense variant G/A;C;T snv 1.2E-04; 8.0E-06 1
rs387906629
GATA2
0.925 0.080 3 128481270 missense variant G/A snv 1
rs387906631
GATA2
0.882 0.080 3 128481901 missense variant G/A snv 2
rs387907097
TGM6
0.925 0.120 20 2417445 missense variant T/G snv 1.5E-04 5.6E-05 1
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 2
rs483352695
TP53
0.882 0.200 17 7674227 missense variant T/A;C;G snv 1
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs569067880
TET2-AS1 ; TET2
0.925 0.080 4 105234864 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs57246956
ELANE
0.882 0.080 19 855649 missense variant G/A;T snv 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs587782529
TP53
0.851 0.200 17 7670700 missense variant G/A;C snv 1
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 1
rs754921650
SETD2
1.000 0.040 3 47120446 missense variant T/C snv 1.2E-05 2.1E-05 1
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 1