VIT
vitrin
Summary
This gene encodes an extracellular matrix (ECM) protein. The protein may be associated with cell adhesion and migration. High levels of expression of the protein in specific parts of the brain suggest its likely role in neural development. [provided by RefSeq, Jun 2016]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1666137789 | 2:36,943,529 | C/T | — | uncertain significance |
| rs1279013165 | 2:36,956,575 | T/C | — | uncertain significance |
| rs139300543 | 2:36,958,076 | G/A | intron variant | — |
| rs369770985 | 2:36,970,243 | C/A | — | uncertain significance |
| rs2465854598 | 2:36,970,265 | T/A | — | uncertain significance |
| rs371430298 | 2:36,970,275 | G/A | — | uncertain significance |
| rs138143496 | 2:36,970,307 | A/T | missense variant | — |
| rs2465855552 | 2:36,970,381 | G/C | — | uncertain significance |
| rs202044807 | 2:36,970,386 | G/A | — | uncertain significance |
| rs145711841 | 2:36,976,865 | C/G | intron variant | — |
| rs1668676634 | 2:36,982,119 | T/G | — | uncertain significance |
| rs561381612 | 2:36,982,144 | A/G | — | uncertain significance |
| rs768117962 | 2:36,982,167 | C/A | — | uncertain significance |
| rs927057909 | 2:36,982,171 | G/T | — | uncertain significance |
| rs78846063 | 2:36,993,295 | C/T | intron variant | — |
| rs769935847 | 2:36,994,255 | A/G | — | uncertain significance |
| rs1177990792 | 2:36,994,332 | G/A | — | uncertain significance |
| rs776405103 | 2:36,994,336 | C/G | — | uncertain significance |
| rs149089705 | 2:36,994,379 | C/T | — | likely benign |
| rs1000916013 | 2:36,994,387 | T/C | — | uncertain significance |
| rs527609274 | 2:36,998,386 | G/A | — | — |
| rs140104536 | 2:37,000,956 | C/G | — | benign |
| rs756000757 | 2:37,002,166 | C/T | — | uncertain significance |
| rs141908607 | 2:37,002,210 | G/C | — | likely benign |
| rs10451640 | 2:37,004,029 | G/A | intron variant | — |
| rs1268335898 | 2:37,008,897 | C/T | — | uncertain significance |
| rs149718553 | 2:37,010,513 | A/G | — | uncertain significance |
| rs1200404252 | 2:37,014,280 | A/G | — | likely benign |
| rs367662837 | 2:37,014,290 | C/T | — | uncertain significance |
| rs756289698 | 2:37,014,308 | G/A | — | uncertain significance |
| rs757475855 | 2:37,014,317 | T/A | — | uncertain significance |
| rs748465900 | 2:37,014,325 | C/T | — | uncertain significance |
| rs2465280315 | 2:37,014,365 | C/A | — | uncertain significance |
| rs386352378 | 2:37,014,392 | G/T | — | uncertain significance |
| rs772641746 | 2:37,014,404 | G/A | — | uncertain significance |
| rs773547450 | 2:37,028,491 | G/A | — | likely benign |
| rs374767207 | 2:37,032,595 | T/C | — | uncertain significance |
| rs766140924 | 2:37,032,606 | G/C | — | uncertain significance |
| rs751099256 | 2:37,032,626 | A/G | — | uncertain significance |
| rs757724129 | 2:37,032,640 | G/A | — | uncertain significance |
| rs374165713 | 2:37,032,758 | C/G | — | uncertain significance |
| rs200166114 | 2:37,032,796 | T/A | missense variant | — |
| rs372368369 | 2:37,032,797 | T/A | — | uncertain significance |
| rs1456157974 | 2:37,032,803 | A/C | — | uncertain significance |
| rs372653959 | 2:37,035,648 | C/T | — | uncertain significance |
| rs149316999 | 2:37,035,864 | A/G | — | uncertain significance |
| rs781780147 | 2:37,035,867 | C/T | — | uncertain significance |
| rs146011119 | 2:37,035,891 | T/A | — | uncertain significance |
| rs910520669 | 2:37,035,913 | G/A | — | uncertain significance |
| rs757456741 | 2:37,035,918 | G/A | — | uncertain significance |
| rs762625146 | 2:37,035,994 | G/T | — | uncertain significance |
| rs770609958 | 2:37,036,071 | A/T | — | uncertain significance |
| rs34099970 | 2:37,036,076 | C/A | — | uncertain significance |
| rs185199684 | 2:37,036,077 | G/C | — | uncertain significance |
| rs767426468 | 2:37,036,095 | G/A | — | uncertain significance |
| rs756105270 | 2:37,036,098 | C/T | — | uncertain significance |
| rs200500702 | 2:37,036,099 | G/A | — | uncertain significance |
| rs57817021 | 2:37,038,075 | C/T | intron variant | — |
| rs147923021 | 2:37,041,338 | A/G | — | uncertain significance |
| rs141772569 | 2:37,041,341 | C/T | — | uncertain significance |
| rs369279118 | 2:37,041,415 | T/C | — | uncertain significance |
| rs138223173 | 2:37,041,426 | G/C | — | uncertain significance |
| rs138832628 | 2:37,041,436 | C/T | — | uncertain significance |
| rs908085770 | 2:37,041,440 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.