RAB37
RAB37, member RAS oncogene family
Summary
Rab proteins are low molecular mass GTPases that are critical regulators of vesicle trafficking. For additional background information on Rab proteins, see MIM 179508.[supplied by OMIM, Apr 2006]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs185756225 | 17:72,666,736 | G/A | downstream gene variant | — |
| rs9904078 | 17:72,667,020 | G/C | — | — |
| rs145126625 | 17:72,670,210 | A/G | intron variant | — |
| rs377519040 | 17:72,676,630 | A/C | — | — |
| rs9916458 | 17:72,688,028 | G/C | — | — |
| rs2034309 | 17:72,688,065 | C/T | downstream gene variant | — |
| rs5018106 | 17:72,712,389 | T/C | upstream gene variant | — |
| rs572318117 | 17:72,716,895 | G/C | — | — |
| rs1868057 | 17:72,716,902 | C/A | — | — |
| rs182817970 | 17:72,720,339 | C/T | intron variant | — |
| rs762798603 | 17:72,733,173 | G/A | — | uncertain significance |
| rs1419074013 | 17:72,733,174 | G/A | — | likely benign |
| rs752805663 | 17:72,733,176 | G/A | — | uncertain significance |
| rs1347396837 | 17:72,733,236 | G/A | — | uncertain significance |
| rs1191012691 | 17:72,736,910 | A/T | — | uncertain significance |
| rs2034593658 | 17:72,736,914 | T/C | — | uncertain significance |
| rs146770958 | 17:72,736,999 | C/G | — | likely benign |
| rs145019795 | 17:72,738,417 | G/A | — | likely benign |
| rs759107202 | 17:72,739,293 | G/A | — | uncertain significance |
| rs760647591 | 17:72,739,299 | G/A | — | uncertain significance |
| rs370945537 | 17:72,739,468 | G/A | — | uncertain significance |
| rs200513132 | 17:72,740,457 | C/A | — | uncertain significance |
| rs772174577 | 17:72,740,478 | A/C | — | uncertain significance |
| rs762014090 | 17:72,740,487 | T/C | — | uncertain significance |
| rs58713971 | 17:72,740,769 | T/G | regulatory region variant | — |
| rs748208881 | 17:72,741,013 | C/T | — | uncertain significance |
| rs773354446 | 17:72,741,020 | G/A | — | uncertain significance |
| rs137872401 | 17:72,741,027 | G/A | — | uncertain significance |
| rs774889397 | 17:72,741,045 | G/A | — | uncertain significance |
| rs374935761 | 17:72,741,067 | G/A | — | uncertain significance |
| rs765394498 | 17:72,741,458 | C/T | — | uncertain significance |
| rs139440620 | 17:72,741,464 | G/A | — | uncertain significance |
| rs200335281 | 17:72,741,468 | A/G | — | likely benign |
| rs763884748 | 17:72,741,498 | G/A | — | uncertain significance |
| rs201555817 | 17:72,741,539 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.