Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 2
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 2
rs35187787
CDH1
0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 1
rs780759537
CDH1
1.000 0.080 16 68822082 missense variant G/A snv 1.6E-05 4.2E-05 1
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 1
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs768678989
MET
1.000 0.080 7 116771932 missense variant C/T snv 2.8E-05 1
rs771333219
MET
1.000 0.080 7 116759444 missense variant C/T snv 1.2E-04 8.4E-05 1
rs63749803
MLH1
1.000 0.080 3 37004421 missense variant T/C;G snv 1
rs63750297
MLH1
1.000 0.080 3 37004412 missense variant C/A;G;T snv 8.0E-06 1
rs63751047
MLH1
1.000 0.080 3 37048525 missense variant C/A;G snv 1
rs63750623
MSH2
0.925 0.160 2 47480707 stop gained C/G;T snv 1
rs63750709
MSH2
0.925 0.160 2 47480846 missense variant C/G;T snv 4.0E-06 1
rs63750795
MSH2
1.000 0.080 2 47480854 missense variant T/G snv 1
rs63750966
MSH2
1.000 0.080 2 47403240 missense variant G/A;C;T snv 1
rs63751400
MSH2
1.000 0.080 2 47480839 missense variant C/G;T snv 4.0E-06 1
rs79777494
MUTYH
0.882 0.120 1 45334495 missense variant G/A snv 1.1E-03 4.9E-04 1
rs1371429276
PTPRT
1.000 0.080 20 42472359 missense variant G/A snv 1.4E-05 1
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1