RALGDS
ral guanine nucleotide dissociation stimulator
Summary
Guanine nucleotide dissociation stimulators (GDSs, or exchange factors), such as RALGDS, are effectors of Ras-related GTPases (see MIM 190020) that participate in signaling for a variety of cellular processes.[supplied by OMIM, Nov 2010]
Known Variants92 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs764693552 | 9:135,973,987 | T/C | — | uncertain significance |
| rs781302534 | 9:135,973,996 | T/C | — | uncertain significance |
| rs1830601292 | 9:135,974,008 | T/C | — | uncertain significance |
| rs1743006719 | 9:135,974,038 | C/G | — | uncertain significance |
| rs747935608 | 9:135,974,039 | C/T | — | uncertain significance |
| rs145020652 | 9:135,974,040 | G/A | — | likely benign |
| rs745773402 | 9:135,974,124 | G/A | — | likely benign |
| rs780791091 | 9:135,974,132 | T/C | — | uncertain significance |
| rs35200098 | 9:135,975,698 | C/T | — | benign |
| rs771418767 | 9:135,975,714 | T/C | — | uncertain significance |
| rs1204917225 | 9:135,975,752 | C/T | — | uncertain significance |
| rs146816334 | 9:135,976,303 | G/A | intron variant | — |
| rs150849255 | 9:135,976,939 | C/G | — | uncertain significance |
| rs78318344 | 9:135,976,976 | C/T | — | benign |
| rs377526998 | 9:135,977,021 | T/C | — | likely benign |
| rs1830762391 | 9:135,977,050 | C/T | — | likely benign |
| rs777411574 | 9:135,977,116 | T/A | — | uncertain significance |
| rs146190679 | 9:135,977,123 | G/A | — | likely benign |
| rs548531503 | 9:135,977,357 | C/T | — | uncertain significance |
| rs774681232 | 9:135,977,381 | C/T | — | uncertain significance |
| rs140751236 | 9:135,977,382 | G/A | — | benign |
| rs35831936 | 9:135,977,400 | G/A | — | benign |
| rs373357690 | 9:135,977,404 | G/A | — | uncertain significance |
| rs147006349 | 9:135,977,426 | C/T | — | uncertain significance |
| rs376306097 | 9:135,977,435 | C/T | — | uncertain significance |
| rs925942592 | 9:135,977,472 | G/A | — | likely benign |
| rs748411421 | 9:135,977,524 | C/T | — | uncertain significance |
| rs201385367 | 9:135,977,873 | G/A | — | uncertain significance |
| rs143632195 | 9:135,977,887 | G/A | — | uncertain significance |
| rs35123849 | 9:135,977,925 | G/A | — | benign |
| rs373186793 | 9:135,978,184 | C/T | — | uncertain significance |
| rs146390575 | 9:135,978,185 | G/A | — | uncertain significance |
| rs200859688 | 9:135,978,227 | C/T | — | likely benign |
| rs143373682 | 9:135,978,228 | G/A | — | benign |
| rs1468529104 | 9:135,978,281 | C/T | — | uncertain significance |
| rs752622189 | 9:135,979,139 | G/T | — | uncertain significance |
| rs151011537 | 9:135,979,659 | C/T | — | likely benign |
| rs200445674 | 9:135,979,669 | T/C | — | uncertain significance |
| rs758724330 | 9:135,981,392 | C/T | — | uncertain significance |
| rs150763247 | 9:135,982,064 | G/A | — | benign |
| rs770902456 | 9:135,982,066 | G/A | — | uncertain significance |
| rs187420525 | 9:135,982,142 | C/T | — | likely benign |
| rs1353529712 | 9:135,982,521 | T/C | — | uncertain significance |
| rs139454388 | 9:135,982,604 | C/T | — | likely benign |
| rs1831111381 | 9:135,982,665 | G/A | — | uncertain significance |
| rs368420692 | 9:135,982,667 | C/T | — | likely benign |
| rs142772650 | 9:135,983,408 | A/G | — | benign |
| rs201185976 | 9:135,983,452 | C/T | — | uncertain significance |
| rs34054856 | 9:135,983,453 | G/C | — | uncertain significance |
| rs139509087 | 9:135,983,471 | T/A | — | likely benign |
| rs750140547 | 9:135,983,505 | G/A | — | likely benign |
| rs753240581 | 9:135,983,625 | T/C | — | uncertain significance |
| rs1473621060 | 9:135,983,700 | G/C | — | uncertain significance |
| rs374513332 | 9:135,983,712 | G/C | — | likely benign |
| rs1223961378 | 9:135,983,746 | C/T | — | uncertain significance |
| rs973144363 | 9:135,983,766 | G/A | — | uncertain significance |
| rs556188646 | 9:135,983,782 | C/T | — | uncertain significance |
| rs747828890 | 9:135,984,077 | A/G | — | likely benign |
| rs34431085 | 9:135,984,085 | C/T | — | benign |
| rs201194989 | 9:135,984,100 | G/C | — | likely benign |
| rs775837663 | 9:135,984,123 | G/A | — | uncertain significance |
| rs531452456 | 9:135,984,157 | G/A | — | likely benign |
| rs140573248 | 9:135,984,173 | T/C | — | likely benign |
| rs561888919 | 9:135,984,208 | C/A | — | uncertain significance |
| rs367807822 | 9:135,985,044 | C/T | — | uncertain significance |
| rs138337653 | 9:135,985,045 | G/A | — | benign |
| rs138259585 | 9:135,985,068 | C/T | — | uncertain significance |
| rs769932363 | 9:135,985,079 | G/A | — | uncertain significance |
| rs763135443 | 9:135,985,082 | G/A | — | uncertain significance |
| rs1447532901 | 9:135,985,089 | G/C | — | uncertain significance |
| rs149649229 | 9:135,985,104 | C/T | — | likely benign |
| rs140586035 | 9:135,985,773 | T/C | — | benign |
| rs763677226 | 9:135,985,780 | C/T | — | uncertain significance |
| rs751265553 | 9:135,985,782 | G/A | — | uncertain significance |
| rs139361973 | 9:135,987,432 | G/A | — | likely benign |
| rs764203868 | 9:135,987,434 | G/C | — | uncertain significance |
| rs367554386 | 9:135,987,458 | C/T | — | uncertain significance |
| rs62638720 | 9:135,987,471 | C/A | — | benign |
| rs528943671 | 9:135,992,870 | C/T | — | — |
| rs915754528 | 9:135,996,420 | T/C | — | uncertain significance |
| rs2490638817 | 9:135,996,426 | A/C | — | uncertain significance |
| rs777637593 | 9:135,996,489 | G/T | — | uncertain significance |
| rs1229743797 | 9:135,996,498 | C/A | — | uncertain significance |
| rs1159362869 | 9:135,996,528 | A/G | — | uncertain significance |
| rs546488917 | 9:135,998,896 | A/G | — | — |
| rs55950819 | 9:135,999,208 | C/T | — | — |
| rs13292214 | 9:135,999,378 | C/G | — | — |
| rs650066 | 9:136,006,115 | A/C | — | — |
| rs772873336 | 9:136,006,435 | G/A | — | likely benign |
| rs472813 | 9:136,014,284 | A/G | intron variant | — |
| rs776747723 | 9:136,024,352 | G/T | — | uncertain significance |
| rs3888561 | 9:136,025,460 | G/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.