SHROOM3
shroom family member 3
Summary
This gene encodes a PDZ-domain-containing protein that belongs to a family of Shroom-related proteins. This protein may be involved in regulating cell shape in certain tissues. A similar protein in mice is required for proper neurulation. [provided by RefSeq, Jan 2011]
Known Variants233 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10000169 | 4:77,356,246 | C/T | — | benign |
| rs79606629 | 4:77,357,198 | T/A | — | benign |
| rs751506162 | 4:77,357,216 | C/A | — | uncertain significance |
| rs142735873 | 4:77,357,273 | G/A | — | uncertain significance |
| rs765592446 | 4:77,357,279 | A/G | — | uncertain significance |
| rs1730559371 | 4:77,357,293 | G/A | — | uncertain significance |
| rs554755626 | 4:77,357,492 | C/A | — | benign |
| rs189707263 | 4:77,357,498 | G/T | — | benign |
| rs11944802 | 4:77,357,528 | G/T | — | benign |
| rs10019833 | 4:77,357,592 | T/C | — | benign |
| rs9992101 | 4:77,360,431 | G/A | intron variant | — |
| rs55940751 | 4:77,365,891 | C/A | — | — |
| rs17319721 | 4:77,368,847 | G/A | regulatory region variant | benign |
| rs1398018 | 4:77,372,923 | T/A | — | — |
| rs6838416 | 4:77,378,829 | G/T | — | — |
| rs28394165 | 4:77,394,018 | T/C | intron variant | — |
| rs11722924 | 4:77,396,854 | G/C | intron variant | — |
| rs10032549 | 4:77,398,015 | A/G | intron variant | — |
| rs4859681 | 4:77,399,164 | C/A | intron variant | — |
| rs28817415 | 4:77,401,452 | C/T | intron variant | — |
| rs188747364 | 4:77,405,599 | C/T | intron variant | — |
| rs7656186 | 4:77,409,818 | C/T | downstream gene variant | — |
| rs4859682 | 4:77,410,318 | C/A | downstream gene variant | — |
| rs10029777 | 4:77,411,030 | C/T | downstream gene variant | — |
| rs10029860 | 4:77,411,101 | C/A | downstream gene variant | — |
| rs2137154 | 4:77,411,501 | C/G | downstream gene variant | — |
| rs2137153 | 4:77,411,660 | G/T | — | — |
| rs13146163 | 4:77,412,091 | G/T | downstream gene variant | — |
| rs13146355 | 4:77,412,140 | G/A | downstream gene variant | — |
| rs7676094 | 4:77,412,894 | C/G | — | — |
| rs7674982 | 4:77,412,997 | G/C | — | — |
| rs7675217 | 4:77,413,142 | G/C | downstream gene variant | — |
| rs12512288 | 4:77,416,817 | C/G | upstream gene variant | — |
| rs13106227 | 4:77,418,681 | G/A | upstream gene variant | — |
| rs13106413 | 4:77,418,698 | G/A | — | — |
| rs11730486 | 4:77,418,968 | G/A | upstream gene variant | — |
| rs4859683 | 4:77,419,073 | C/A | — | — |
| rs4493564 | 4:77,420,407 | A/G | intron variant | — |
| rs1986734 | 4:77,420,784 | C/T | regulatory region variant | — |
| rs4447885 | 4:77,422,171 | A/G | intron variant | — |
| rs73826207 | 4:77,439,072 | G/A | intron variant | — |
| rs10010562 | 4:77,456,022 | A/T | — | — |
| rs144435434 | 4:77,476,772 | G/T | — | benign |
| rs770324004 | 4:77,476,789 | C/G | — | likely benign |
| rs75039400 | 4:77,476,809 | T/C | — | benign |
| rs144913986 | 4:77,476,909 | G/C | — | likely benign |
| rs747862563 | 4:77,476,912 | C/T | — | uncertain significance |
| rs4263424 | 4:77,512,141 | A/C | regulatory region variant | — |
| rs28416132 | 4:77,529,816 | T/G | — | — |
| rs62300927 | 4:77,532,524 | G/A | regulatory region variant | — |
| rs56281442 | 4:77,533,939 | A/G | intron variant | — |
| rs13125913 | 4:77,535,836 | A/T | — | — |
| rs143141511 | 4:77,568,991 | G/A | downstream gene variant | — |
| rs141053179 | 4:77,589,911 | C/G | intron variant | — |
| rs753102566 | 4:77,631,386 | C/A | — | uncertain significance |
| rs201518979 | 4:77,631,391 | C/T | — | uncertain significance |
| rs200571114 | 4:77,631,403 | G/A | — | uncertain significance |
| rs3821979 | 4:77,631,425 | T/A | — | benign |
| rs768503568 | 4:77,631,427 | C/T | — | uncertain significance |
| rs145112769 | 4:77,652,057 | G/C | — | benign |
| rs344135 | 4:77,652,219 | T/C | — | benign |
| rs344139 | 4:77,659,090 | T/A | — | — |
| rs932668101 | 4:77,659,936 | A/C | — | uncertain significance |
| rs139272770 | 4:77,659,945 | C/T | — | benign |
| rs542556063 | 4:77,659,961 | G/A | — | uncertain significance |
| rs766219406 | 4:77,659,973 | A/G | — | likely benign |
| rs377199268 | 4:77,660,023 | C/A | — | likely benign |
| rs747723693 | 4:77,660,056 | G/A | — | likely benign |
| rs1411090305 | 4:77,660,074 | A/T | — | uncertain significance |
| rs149686763 | 4:77,660,093 | G/A | — | uncertain significance |
| rs374710074 | 4:77,660,148 | C/A | — | uncertain significance |
| rs344140 | 4:77,660,162 | C/G | — | benign |
| rs1364692499 | 4:77,660,182 | A/G | — | uncertain significance |
| rs2476034954 | 4:77,660,216 | A/C | — | uncertain significance |
| rs61999292 | 4:77,660,299 | G/T | — | benign |
| rs554492056 | 4:77,660,380 | C/T | — | uncertain significance |
| rs146652221 | 4:77,660,381 | G/A | — | likely benign |
| rs776679144 | 4:77,660,384 | G/A | — | uncertain significance |
| rs200716219 | 4:77,660,393 | T/C | — | likely benign |
| rs145159967 | 4:77,660,427 | T/G | — | likely benign |
| rs761601802 | 4:77,660,502 | C/G | — | uncertain significance |
| rs200056000 | 4:77,660,503 | G/A | — | uncertain significance |
| rs755595009 | 4:77,660,512 | C/T | — | uncertain significance |
| rs201142744 | 4:77,660,519 | G/A | — | uncertain significance |
| rs775627642 | 4:77,660,543 | G/A | — | uncertain significance |
| rs61745983 | 4:77,660,550 | T/C | — | benign |
| rs1284623372 | 4:77,660,555 | A/C | — | uncertain significance |
| rs2476035799 | 4:77,660,556 | A/T | — | uncertain significance |
| rs148120221 | 4:77,660,566 | C/T | — | uncertain significance |
| rs141874410 | 4:77,660,589 | C/T | — | likely benign |
| rs572629061 | 4:77,660,672 | A/G | — | uncertain significance |
| rs2476036107 | 4:77,660,676 | T/A | — | uncertain significance |
| rs373907641 | 4:77,660,694 | C/G | — | likely benign |
| rs756962293 | 4:77,660,707 | C/A | — | uncertain significance |
| rs344141 | 4:77,660,731 | G/C | — | benign |
| rs764124002 | 4:77,660,734 | G/C | — | uncertain significance |
| rs774107763 | 4:77,660,739 | T/G | — | likely benign |
| rs1049485785 | 4:77,660,789 | A/G | — | uncertain significance |
| rs769406699 | 4:77,660,845 | G/A | — | uncertain significance |
| rs748852718 | 4:77,660,858 | T/C | — | uncertain significance |
Showing 100 of 233 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.