PTCSC2
papillary thyroid carcinoma susceptibility candidate 2
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10817938 | 9:100,462,409 | T/C | coding sequence variant | — |
| rs16924016 | 9:100,511,331 | C/T | regulatory region variant | — |
| rs7030256 | 9:100,535,203 | C/G | intergenic variant | — |
| rs7028661 | 9:100,538,470 | A/G | intergenic variant | — |
| rs112817873 | 9:100,539,518 | A/T | — | — |
| rs7021576 | 9:100,540,541 | C/T | intergenic variant | — |
| rs7847663 | 9:100,544,868 | C/A | — | — |
| rs1561962 | 9:100,546,219 | C/T | intergenic variant | — |
| rs925489 | 9:100,546,600 | C/G | — | — |
| rs7032019 | 9:100,548,144 | G/C | — | — |
| rs7864322 | 9:100,548,934 | C/T | regulatory region variant | — |
| rs7850258 | 9:100,549,013 | A/G | regulatory region variant | — |
| rs1443438 | 9:100,550,028 | T/C | intergenic variant | — |
| rs7030241 | 9:100,550,375 | T/G | — | — |
| rs7027030 | 9:100,550,455 | A/G | — | — |
| rs12352658 | 9:100,551,768 | G/C | — | — |
| rs7847449 | 9:100,551,908 | C/A | regulatory region variant | — |
| rs965513 | 9:100,556,109 | A/T | — | — |
| rs10759944 | 9:100,556,972 | A/G | intergenic variant | — |
| rs13295081 | 9:100,559,011 | T/C | intergenic variant | — |
| rs13290258 | 9:100,559,093 | C/G | — | — |
| rs10818090 | 9:100,561,486 | C/T | regulatory region variant | — |
| rs7045138 | 9:100,591,463 | C/G | — | — |
| rs7048394 | 9:100,605,433 | T/C | intergenic variant | — |
| rs894673 | 9:100,612,270 | A/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.