Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 5
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs11762469
BRAF
1.000 0.080 7 140914412 intron variant A/G;T snv 1
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 1
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs2622590
XKR4
0.925 0.080 8 55445714 intron variant G/A snv 0.15 3
rs1562430
PCAT1 ; CASC8 ; CASC21 ; POU5F1B
0.807 0.160 8 127375606 intron variant T/C snv 0.41 2
rs6996585
NRG1
0.925 0.080 8 32543285 intron variant A/G snv 0.37 2
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54 1
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 5
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 1
rs1867277
PTCSC2 ; FOXE1
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 1
rs72753537
TRMO ; LOC112268051
1.000 0.080 9 97898464 intergenic variant T/C snv 9.4E-02 1
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 18
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 14
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 10
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 10
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 7
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 7
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 4