Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 86
rs35697691 15 52061301 missense variant C/G snv 5.8E-02 5.9E-02 3
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs877610 1.000 17 3572196 synonymous variant C/T snv 4.6E-02 7.5E-02 3
rs11671784 0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02 9
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 15
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs141613848 0.925 0.080 17 74768481 missense variant A/T snv 1.0E-03 1.2E-03 4
rs377767426
RET
1.000 0.080 10 43119694 missense variant C/G snv 1.8E-04 1.0E-04 2
rs201701502 0.851 0.080 1 162775837 missense variant C/G;T snv 1.5E-04 2.1E-05 5
rs771086543 10 102422814 missense variant G/A snv 1.3E-04 1.0E-04 1
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 21
rs80338948 0.763 0.280 13 20189155 missense variant G/A snv 1.2E-04 2.0E-04 3
rs367569800 3 127014358 missense variant G/A;C snv 6.7E-05; 1.0E-04 1
rs387906698 0.827 0.040 7 142751919 missense variant C/A;T snv 4.0E-06; 7.2E-05 8
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs121917887 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs377444977 0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs757786591 2 218890134 missense variant G/A snv 4.4E-05 2.1E-05 1
rs3918252 20 46010492 missense variant C/G snv 3.6E-05 2.4E-04 1
rs760101437 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs367827951 8 42182000 missense variant G/A;C snv 4.0E-06; 2.8E-05 1
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs587782359 1.000 0.080 16 68812244 missense variant C/G;T snv 2.8E-05 3