Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227869 0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9
rs763538721 0.807 0.160 14 61740897 missense variant T/A snv 4.0E-06 8
rs778212685 0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs1064795638 0.851 0.080 3 52403251 stop gained G/A snv 7
rs1169803481 0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 7
rs768827923 0.851 0.080 1 9721816 missense variant T/G snv 6
rs776935407 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 6
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
rs1800858
RET
0.851 0.160 10 43100520 synonymous variant A/C;G snv 0.73 4
rs768891111 0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs907580 0.851 0.080 9 97860315 downstream gene variant T/A;C;G snv 4
rs1031583860 0.882 0.080 11 58709815 missense variant T/C snv 3
rs2708896 0.882 0.080 7 47955186 upstream gene variant T/C;G snv 3
rs747463591 0.882 0.080 10 59906391 missense variant C/A;G;T snv 4.9E-06; 9.9E-06 3
rs78929565 0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs1032006770 0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1365943053 0.882 0.080 9 95516630 missense variant C/T snv 7.0E-06 3
rs1297812518 0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9
rs1248131654 0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05 4
rs145475805
TG
0.882 0.080 8 132887509 missense variant A/G snv 8.8E-05 3.3E-04 4
rs779791579 0.882 0.080 9 95508325 missense variant G/C snv 7.8E-04 6.1E-04 3
rs63750447 0.716 0.200 3 37025749 missense variant T/A snv 2.7E-03 7.5E-04 17
rs78201625 0.851 0.080 10 113577182 missense variant C/T snv 2.4E-03 1.8E-03 4