TNN
tenascin N
Summary
Predicted to enable integrin binding activity. Involved in positive regulation of sprouting angiogenesis; regulation of cell adhesion; and regulation of cell migration. Located in collagen-containing extracellular matrix. Part of tenascin complex. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs142139120 | 1:175,046,627 | C/A | — | uncertain significance |
| rs749351472 | 1:175,046,658 | A/G | — | uncertain significance |
| rs372288697 | 1:175,046,664 | A/C | — | uncertain significance |
| rs2528919607 | 1:175,046,708 | A/C | — | uncertain significance |
| rs201940821 | 1:175,046,886 | G/A | — | uncertain significance |
| rs145009218 | 1:175,046,920 | G/A | — | uncertain significance |
| rs769031518 | 1:175,046,943 | G/A | — | uncertain significance |
| rs745575208 | 1:175,048,471 | C/A | — | uncertain significance |
| rs200816440 | 1:175,048,580 | C/T | — | uncertain significance |
| rs765430450 | 1:175,048,657 | C/A | — | uncertain significance |
| rs765864058 | 1:175,048,681 | G/A | — | uncertain significance |
| rs375734720 | 1:175,048,730 | T/C | — | likely benign |
| rs764490910 | 1:175,048,747 | G/A | — | uncertain significance |
| rs768862831 | 1:175,048,803 | C/G | — | uncertain significance |
| rs535429156 | 1:175,048,834 | T/A | — | uncertain significance |
| rs747487606 | 1:175,049,305 | C/A | — | uncertain significance |
| rs761592638 | 1:175,049,380 | A/T | — | uncertain significance |
| rs760414627 | 1:175,049,385 | T/C | — | uncertain significance |
| rs765420132 | 1:175,049,392 | T/C | — | uncertain significance |
| rs747596869 | 1:175,049,415 | G/A | — | uncertain significance |
| rs756402472 | 1:175,052,887 | C/A | — | uncertain significance |
| rs370497014 | 1:175,052,901 | G/T | — | uncertain significance |
| rs138630687 | 1:175,052,999 | A/G | — | uncertain significance |
| rs1174496896 | 1:175,053,001 | G/A | — | uncertain significance |
| rs758464012 | 1:175,054,582 | A/C | — | uncertain significance |
| rs201015182 | 1:175,054,607 | C/T | — | uncertain significance |
| rs2528941294 | 1:175,054,618 | A/T | — | uncertain significance |
| rs6664276 | 1:175,054,626 | G/T | — | benign |
| rs191704337 | 1:175,054,959 | G/A | intron variant | — |
| rs143661378 | 1:175,063,176 | G/A | — | uncertain significance |
| rs765018662 | 1:175,063,182 | G/A | — | uncertain significance |
| rs75181012 | 1:175,063,267 | T/C | — | uncertain significance |
| rs780059277 | 1:175,063,285 | G/C | — | uncertain significance |
| rs2525640054 | 1:175,063,308 | C/G | — | uncertain significance |
| rs138714660 | 1:175,063,360 | G/T | — | uncertain significance |
| rs199888967 | 1:175,063,378 | A/G | — | uncertain significance |
| rs141767103 | 1:175,066,567 | G/T | — | uncertain significance |
| rs146035631 | 1:175,066,568 | C/T | — | uncertain significance |
| rs750909748 | 1:175,066,620 | C/A | — | uncertain significance |
| rs2149433109 | 1:175,067,546 | C/T | — | uncertain significance |
| rs1332144028 | 1:175,067,576 | C/T | — | uncertain significance |
| rs756343208 | 1:175,067,651 | C/T | — | uncertain significance |
| rs759202941 | 1:175,067,672 | A/C | — | uncertain significance |
| rs147445406 | 1:175,067,723 | C/A | — | uncertain significance |
| rs560076374 | 1:175,069,805 | G/A | — | — |
| rs192134401 | 1:175,079,424 | G/A | intron variant | — |
| rs755320265 | 1:175,086,080 | G/T | — | uncertain significance |
| rs768342181 | 1:175,086,168 | A/G | — | uncertain significance |
| rs373529382 | 1:175,086,189 | C/A | — | uncertain significance |
| rs918315348 | 1:175,086,263 | G/T | — | uncertain significance |
| rs543482646 | 1:175,086,276 | C/T | — | uncertain significance |
| rs775708244 | 1:175,086,303 | C/T | — | uncertain significance |
| rs768981140 | 1:175,086,326 | A/G | — | uncertain significance |
| rs549739444 | 1:175,087,894 | A/G | — | uncertain significance |
| rs757458812 | 1:175,087,895 | C/T | — | uncertain significance |
| rs187636582 | 1:175,088,774 | C/T | intron variant | — |
| rs2525707703 | 1:175,092,562 | A/G | — | uncertain significance |
| rs61746976 | 1:175,092,638 | G/A | — | uncertain significance |
| rs148646044 | 1:175,092,794 | A/G | — | uncertain significance |
| rs763318923 | 1:175,096,096 | G/A | — | uncertain significance |
| rs368231525 | 1:175,096,126 | G/A | — | uncertain significance |
| rs147363762 | 1:175,096,157 | C/T | — | uncertain significance |
| rs149726222 | 1:175,096,162 | C/A | — | uncertain significance |
| rs750454496 | 1:175,096,200 | G/T | — | uncertain significance |
| rs377367173 | 1:175,097,740 | G/A | — | uncertain significance |
| rs200234361 | 1:175,097,757 | G/T | — | uncertain significance |
| rs765803389 | 1:175,097,826 | G/A | — | uncertain significance |
| rs144117200 | 1:175,097,831 | C/G | — | uncertain significance |
| rs747972743 | 1:175,097,868 | G/A | — | uncertain significance |
| rs149018237 | 1:175,097,881 | T/C | — | uncertain significance |
| rs546877646 | 1:175,104,993 | C/T | — | uncertain significance |
| rs73030994 | 1:175,104,994 | G/A | — | uncertain significance |
| rs1347221879 | 1:175,105,075 | T/A | — | uncertain significance |
| rs762663051 | 1:175,105,986 | G/C | — | uncertain significance |
| rs748546693 | 1:175,106,025 | A/G | — | uncertain significance |
| rs200935300 | 1:175,106,035 | A/G | — | uncertain significance |
| rs1407403021 | 1:175,106,077 | G/A | — | uncertain significance |
| rs199923075 | 1:175,106,086 | G/A | — | uncertain significance |
| rs10912894 | 1:175,106,616 | T/C | intron variant | — |
| rs751673595 | 1:175,113,585 | G/T | — | uncertain significance |
| rs752282631 | 1:175,113,616 | G/A | — | uncertain significance |
| rs201592719 | 1:175,116,062 | G/T | — | likely benign |
| rs146012416 | 1:175,116,095 | A/G | — | uncertain significance |
| rs12135071 | 1:175,117,548 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.