Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 17
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
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 10
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 10
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 9
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 9
rs77503355
RET
0.776 0.160 10 43113655 missense variant G/A;C;T snv 8
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 8
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 8
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 8
rs377767412
RET
0.790 0.240 10 43114547 synonymous variant G/A snv 7
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 7
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv 6
rs377767429
RET
0.790 0.120 10 43120120 missense variant GC/TT mnv 5
rs75030001
RET
0.807 0.160 10 43118458 missense variant G/C;T snv 4.0E-06; 2.0E-05 4
rs77316810
RET
0.776 0.200 10 43113654 missense variant T/A;C;G snv 4
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 4
rs143795581
RET
0.851 0.120 10 43114596 missense variant A/C;G snv 8.0E-06 3
rs146646971
RET
0.807 0.120 10 43114598 missense variant G/C;T snv 2.4E-05 3
rs79890926
RET
0.827 0.160 10 43113656 missense variant C/G;T snv 1.6E-05 3
rs377767391
RET
0.827 0.160 10 43113627 missense variant T/A;C;G snv 2
rs377767397
RET
0.790 0.280 10 43113628 missense variant G/A;C;T snv 2
rs377767406
RET
0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 2
rs377767436
RET
0.925 0.120 10 43114491 protein altering variant -/ACGAGCTGTGCC delins 2