Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 14
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 11
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 11
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 10
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 9
rs377767412
RET
0.790 0.240 10 43114547 synonymous variant G/A snv 7
rs1564494285
RET
0.882 0.200 10 43111219 frameshift variant TG/- delins 6
rs79890926
RET
0.827 0.160 10 43113656 missense variant C/G;T snv 1.6E-05 5
rs2435357
RET
0.790 0.240 10 43086608 intron variant T/C snv 0.79 3
rs1553540620
MIR3131 ; IHH
1.000 2 219060317 missense variant G/T snv 2
rs1554818362
RET
1.000 10 43109163 missense variant C/T snv 2
rs537874538
RET
1.000 10 43111381 missense variant G/A snv 2.7E-04 5.6E-05 2
rs76397662
RET
0.851 0.200 10 43102345 missense variant G/A snv 7.9E-04 2.9E-04 2
rs76764689
RET
0.925 0.080 10 43100480 missense variant C/T snv 2
rs1057519052
DENND3
1.000 8 141168410 frameshift variant G/- del 1
rs1057519322
NCLN
1.000 19 3193404 stop gained C/T snv 1
rs1057519323
NUP98
1.000 11 3676355 missense variant T/C snv 1
rs533778281
POLR2F
1.000 22 38016774 intron variant G/C snv 9.5E-04 1
rs606231342
POLR2F
1.000 22 38016208 intron variant G/A snv 1.4E-05 1
rs1060499894
RET
1.000 10 43106455 missense variant G/C;T snv 1
rs1255575160
RET
1.000 10 43113672 missense variant C/A snv 4.0E-06 1
rs1318733775
RET
1.000 10 43119576 missense variant G/A snv 4.1E-06 7.0E-06 1
rs1451004715
RET
1.000 10 43120091 missense variant G/A snv 1
rs1477699803
RET
1.000 10 43100662 missense variant G/A snv 1
rs1483605155
RET
1.000 10 43113579 missense variant G/A;C snv 4.1E-06 1