Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs709399 0.882 0.080 14 103701208 3 prime UTR variant G/A snv 0.59 0.61 3
rs747463591 0.882 0.080 10 59906391 missense variant C/A;G;T snv 4.9E-06; 9.9E-06 3
rs779791579 0.882 0.080 9 95508325 missense variant G/C snv 7.8E-04 6.1E-04 3
rs78929565 0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs183334241 0.925 0.080 18 75288186 missense variant G/A;C snv 1.6E-04 2
rs200817352 1.000 0.080 2 113220126 missense variant G/A;C snv 2.0E-03; 4.0E-06 2
rs373646414 1.000 0.080 14 95132574 missense variant T/C snv 1.6E-05 5.6E-05 2
rs377767414
RET
0.925 0.080 10 43118397 missense variant G/A snv 2
rs78081605 0.925 0.080 18 75288051 missense variant G/C snv 8.0E-06 7.0E-06 2
rs11214077 0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs34677591 0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10
rs778212685 0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs360718 0.827 0.120 11 112164016 5 prime UTR variant A/C snv 0.26 5
rs786203472 0.827 0.120 22 28719414 start lost T/C snv 5
rs863224748 0.827 0.120 22 28734721 start lost T/C snv 5
rs1946519 0.851 0.120 11 112164784 intron variant A/C snv 0.60 4
rs377767427
RET
0.882 0.120 10 43120114 missense variant C/G snv 4.0E-06 3
rs147394161 0.925 0.120 1 21598453 missense variant T/C snv 9.5E-03 1.0E-02 2
rs1057519736 0.752 0.160 15 90088605 missense variant C/G snv 13
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs12628 0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34 10
rs1867277 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 10
rs1297812518 0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9