Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 17
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 16
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 15
rs1991517 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 13
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs111033307 0.851 0.240 7 107694473 missense variant T/G snv 1.0E-04 7.7E-05 6
rs2653349 0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06 5
rs377767395
RET
0.882 0.120 10 43113613 missense variant A/G snv 4
rs377767402
RET
0.882 0.120 10 43113663 missense variant G/A snv 2.4E-05 2.8E-05 4
rs55846256
RET
0.882 0.120 10 43114493 missense variant C/A;T snv 4.0E-06; 1.3E-04 4
rs28939086 0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 4
rs4774518 0.925 0.120 15 45117274 stop gained C/G;T snv 1.4E-04; 1.7E-02 3
rs180671269 1.000 0.120 15 45107450 stop gained T/A;C snv 6.8E-04; 4.0E-06 2
rs753012199
TPO
1.000 0.120 2 1477425 missense variant G/A snv 7.0E-06 2
rs368488511 15 45099748 missense variant C/G;T snv 1.9E-04 1
rs140117073 4 7064176 missense variant C/A;G;T snv 4.0E-06; 5.3E-04 1
rs80169463 4 3316336 missense variant G/A;C snv 1.2E-03; 4.0E-06 1