OLFML2B
olfactomedin like 2B
Summary
This gene encodes an olfactomedin domain-containing protein. Most olfactomedin domain-containing proteins are secreted glycoproteins. [provided by RefSeq, Dec 2016]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12039519 | 1:161,953,400 | G/A | 3 prime UTR variant | — |
| rs865787033 | 1:161,953,484 | T/A | — | uncertain significance |
| rs529486618 | 1:161,953,575 | C/T | — | uncertain significance |
| rs771592846 | 1:161,953,688 | A/C | — | uncertain significance |
| rs863224950 | 1:161,953,697 | C/T | missense variant | pathogenic |
| rs551350323 | 1:161,953,712 | C/T | — | uncertain significance |
| rs372811871 | 1:161,953,724 | C/T | — | uncertain significance |
| rs2525652785 | 1:161,953,745 | G/A | — | uncertain significance |
| rs537124627 | 1:161,953,758 | C/T | — | uncertain significance |
| rs569796342 | 1:161,953,808 | T/C | — | uncertain significance |
| rs61737578 | 1:161,953,930 | A/G | — | benign |
| rs776929841 | 1:161,953,967 | T/C | — | uncertain significance |
| rs765357992 | 1:161,953,980 | C/A | — | uncertain significance |
| rs144617718 | 1:161,954,016 | G/A | — | uncertain significance |
| rs200652136 | 1:161,954,049 | A/G | — | uncertain significance |
| rs185436876 | 1:161,954,639 | C/T | missense variant | pathogenic |
| rs749921063 | 1:161,954,657 | C/A | — | uncertain significance |
| rs756430892 | 1:161,954,665 | C/T | missense variant | pathogenic |
| rs863224949 | 1:161,954,701 | C/T | missense variant | pathogenic |
| rs1689550751 | 1:161,954,770 | C/T | — | uncertain significance |
| rs748120973 | 1:161,967,618 | T/C | — | uncertain significance |
| rs141316615 | 1:161,967,626 | C/T | — | uncertain significance |
| rs201010987 | 1:161,967,677 | C/A | — | uncertain significance |
| rs368834766 | 1:161,967,707 | G/A | — | uncertain significance |
| rs141122488 | 1:161,967,711 | C/G | — | uncertain significance |
| rs545383060 | 1:161,967,720 | C/G | — | uncertain significance |
| rs759826217 | 1:161,967,731 | G/A | — | uncertain significance |
| rs863224948 | 1:161,967,783 | C/A | missense variant | pathogenic |
| rs544736438 | 1:161,967,798 | C/T | — | uncertain significance |
| rs749805939 | 1:161,967,803 | G/A | — | uncertain significance |
| rs2525695024 | 1:161,967,824 | G/A | — | uncertain significance |
| rs140535952 | 1:161,967,893 | G/A | — | uncertain significance |
| rs372550662 | 1:161,968,002 | C/T | — | uncertain significance |
| rs142806829 | 1:161,968,031 | C/A | missense variant | uncertain significance |
| rs115147843 | 1:161,968,042 | A/G | — | benign |
| rs863224947 | 1:161,968,050 | G/A | missense variant | pathogenic |
| rs73021254 | 1:161,968,072 | G/A | — | benign |
| rs2525696569 | 1:161,968,075 | G/C | — | uncertain significance |
| rs150924085 | 1:161,969,936 | C/A | — | uncertain significance |
| rs369342795 | 1:161,969,963 | G/A | — | uncertain significance |
| rs141480556 | 1:161,969,990 | G/C | — | uncertain significance |
| rs768505143 | 1:161,970,023 | G/A | — | uncertain significance |
| rs757440341 | 1:161,970,077 | T/C | — | uncertain significance |
| rs750492409 | 1:161,970,098 | C/T | — | uncertain significance |
| rs370849635 | 1:161,970,122 | C/G | — | uncertain significance |
| rs150601301 | 1:161,971,546 | A/G | intron variant | — |
| rs72712100 | 1:161,975,381 | C/T | intron variant | — |
| rs766546387 | 1:161,976,133 | C/T | — | uncertain significance |
| rs767556474 | 1:161,976,149 | T/C | — | uncertain significance |
| rs778489676 | 1:161,976,184 | C/T | — | uncertain significance |
| rs759621817 | 1:161,976,233 | C/T | — | uncertain significance |
| rs368455338 | 1:161,976,253 | T/A | — | uncertain significance |
| rs746284817 | 1:161,987,197 | A/G | — | uncertain significance |
| rs532457018 | 1:161,987,209 | C/T | — | uncertain significance |
| rs374129648 | 1:161,989,779 | G/A | — | uncertain significance |
| rs1690654452 | 1:161,989,845 | T/G | — | uncertain significance |
| rs760409022 | 1:161,989,861 | C/T | — | likely benign |
| rs375915194 | 1:161,989,890 | C/T | — | uncertain significance |
| rs1158737840 | 1:161,989,900 | G/T | — | uncertain significance |
| rs754774247 | 1:161,993,051 | G/A | — | uncertain significance |
| rs759517778 | 1:161,993,126 | G/A | — | uncertain significance |
| rs781712271 | 1:161,993,177 | A/C | missense variant | pathogenic |
| rs146578225 | 1:161,993,187 | C/T | — | uncertain significance |
| rs186197796 | 1:161,993,402 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.