Disease: Thyroid carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 8
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 6
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 6
rs142698837
TG
0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 5
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 4
rs907580 0.851 0.080 9 97860315 downstream gene variant T/A;C;G snv 4
rs10984103 0.925 0.080 9 97876993 TF binding site variant A/C snv 0.68 2
rs7024345
PTCSC2
0.925 0.080 9 97832956 intron variant A/G snv 0.82 2
rs7848973
PTCSC2
0.925 0.080 9 97826557 intron variant A/G snv 0.67 2
rs7866436 0.925 0.080 9 97887814 intergenic variant G/A snv 0.70 2
rs925487 0.925 0.080 9 97874116 regulatory region variant C/A;T snv 2