PLEKHG4B
pleckstrin homology and RhoGEF domain containing G4B
Summary
This gene encodes a large protein that contains a pleckstrin homology domain and may function as a guanine nucleotide exchange factor. [provided by RefSeq, May 2017]
Known Variants133 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1004016678 | 5:140,499 | C/G | — | uncertain significance |
| rs2477023194 | 5:140,534 | G/C | — | uncertain significance |
| rs950170891 | 5:140,564 | C/A | — | uncertain significance |
| rs1033372982 | 5:140,567 | C/T | — | likely benign |
| rs534089227 | 5:140,570 | G/A | — | uncertain significance |
| rs372952064 | 5:140,603 | G/A | — | uncertain significance |
| rs1009283614 | 5:140,624 | A/C | — | uncertain significance |
| rs1383625761 | 5:140,642 | G/A | — | uncertain significance |
| rs1338982037 | 5:140,661 | G/A | — | uncertain significance |
| rs757696280 | 5:140,666 | C/A | — | likely benign |
| rs563445670 | 5:140,682 | C/T | — | uncertain significance |
| rs370207841 | 5:140,712 | C/T | — | uncertain significance |
| rs142896243 | 5:143,213 | G/T | — | uncertain significance |
| rs748381818 | 5:143,221 | C/A | — | uncertain significance |
| rs150711935 | 5:143,227 | G/A | — | uncertain significance |
| rs2477035185 | 5:143,231 | C/A | — | uncertain significance |
| rs771526424 | 5:143,236 | G/A | — | uncertain significance |
| rs759763364 | 5:143,248 | C/T | — | uncertain significance |
| rs115149634 | 5:143,249 | G/A | — | likely benign |
| rs201992233 | 5:143,263 | G/A | — | uncertain significance |
| rs778030834 | 5:143,284 | G/A | — | uncertain significance |
| rs775901223 | 5:143,315 | A/G | — | likely benign |
| rs536040535 | 5:143,329 | G/A | — | uncertain significance |
| rs142208662 | 5:143,490 | C/T | — | benign |
| rs769604175 | 5:143,507 | G/A | — | uncertain significance |
| rs752112236 | 5:143,519 | C/G | — | uncertain significance |
| rs149661863 | 5:143,533 | C/T | — | likely benign |
| rs773974453 | 5:143,536 | A/G | — | uncertain significance |
| rs372761117 | 5:143,587 | C/A | — | uncertain significance |
| rs2477040224 | 5:144,979 | G/A | — | uncertain significance |
| rs148716910 | 5:151,721 | G/A | — | benign |
| rs774394437 | 5:155,055 | C/A | — | uncertain significance |
| rs142824791 | 5:155,476 | C/T | — | uncertain significance |
| rs2477066545 | 5:155,541 | A/G | — | uncertain significance |
| rs559494070 | 5:155,542 | C/T | — | uncertain significance |
| rs773290909 | 5:155,553 | G/T | — | uncertain significance |
| rs1560935276 | 5:156,226 | A/G | — | uncertain significance |
| rs1345048209 | 5:156,274 | G/C | — | uncertain significance |
| rs549220555 | 5:156,282 | C/G | — | uncertain significance |
| rs193920840 | 5:156,288 | C/T | — | uncertain significance |
| rs139467230 | 5:156,904 | G/A | — | uncertain significance |
| rs376301203 | 5:156,923 | G/A | — | likely benign |
| rs754394966 | 5:161,902 | C/G | — | uncertain significance |
| rs572871479 | 5:161,926 | C/T | — | likely benign |
| rs149715797 | 5:161,938 | C/T | — | uncertain significance |
| rs1320878463 | 5:161,940 | C/A | — | uncertain significance |
| rs529537081 | 5:161,944 | G/A | — | likely benign |
| rs754520403 | 5:161,988 | G/A | — | uncertain significance |
| rs199616508 | 5:162,028 | G/A | — | uncertain significance |
| rs372619983 | 5:162,036 | C/T | — | uncertain significance |
| rs763401302 | 5:162,037 | G/A | — | likely benign |
| rs116836100 | 5:162,040 | C/T | — | uncertain significance |
| rs568109142 | 5:162,045 | G/A | — | benign |
| rs1028687862 | 5:162,852 | G/A | — | uncertain significance |
| rs914820013 | 5:162,919 | A/G | — | uncertain significance |
| rs758291323 | 5:162,942 | G/A | — | uncertain significance |
| rs746370171 | 5:162,958 | G/C | — | uncertain significance |
| rs144399749 | 5:162,994 | C/T | — | likely benign |
| rs780993541 | 5:163,000 | C/T | — | uncertain significance |
| rs1362769097 | 5:163,029 | C/T | — | uncertain significance |
| rs140394022 | 5:163,039 | G/A | — | uncertain significance |
| rs116369175 | 5:163,045 | G/A | — | uncertain significance |
| rs1437220998 | 5:163,080 | C/G | — | uncertain significance |
| rs371488650 | 5:163,090 | C/T | — | uncertain significance |
| rs748603403 | 5:163,123 | G/A | — | uncertain significance |
| rs772967343 | 5:163,135 | C/T | — | uncertain significance |
| rs375303944 | 5:163,168 | C/G | — | uncertain significance |
| rs764928944 | 5:163,181 | T/G | — | uncertain significance |
| rs752425552 | 5:163,183 | G/C | — | uncertain significance |
| rs935485691 | 5:163,197 | G/A | — | uncertain significance |
| rs371920681 | 5:163,204 | C/T | — | uncertain significance |
| rs115510931 | 5:163,218 | G/A | — | uncertain significance |
| rs201880786 | 5:163,278 | T/C | — | uncertain significance |
| rs548159739 | 5:163,294 | C/G | — | uncertain significance |
| rs988247000 | 5:163,327 | G/A | — | uncertain significance |
| rs923522979 | 5:163,335 | A/G | — | uncertain significance |
| rs372964740 | 5:163,371 | G/A | — | uncertain significance |
| rs543235181 | 5:163,392 | A/C | — | uncertain significance |
| rs762271174 | 5:163,395 | C/A | — | uncertain significance |
| rs141957182 | 5:163,427 | A/G | — | likely benign |
| rs146828185 | 5:163,429 | A/T | — | uncertain significance |
| rs774992503 | 5:163,581 | C/T | — | uncertain significance |
| rs1311361780 | 5:163,595 | G/C | — | uncertain significance |
| rs201285914 | 5:163,599 | C/T | — | uncertain significance |
| rs2477093304 | 5:163,642 | A/G | — | uncertain significance |
| rs746658573 | 5:163,657 | T/C | — | likely benign |
| rs371026077 | 5:169,460 | G/A | — | uncertain significance |
| rs75579589 | 5:169,512 | G/A | — | benign |
| rs1236845440 | 5:169,513 | T/C | — | uncertain significance |
| rs143269875 | 5:169,525 | G/A | — | uncertain significance |
| rs148185735 | 5:169,580 | G/A | — | uncertain significance |
| rs139086978 | 5:169,649 | G/A | — | uncertain significance |
| rs542193129 | 5:169,660 | C/G | — | uncertain significance |
| rs116480186 | 5:171,339 | G/A | — | benign |
| rs2477120142 | 5:171,359 | G/T | — | uncertain significance |
| rs760278254 | 5:171,381 | G/A | — | uncertain significance |
| rs772299873 | 5:171,437 | G/A | — | uncertain significance |
| rs151048083 | 5:171,480 | G/A | — | uncertain significance |
| rs773157851 | 5:171,518 | G/A | — | uncertain significance |
| rs368490985 | 5:171,522 | A/G | — | uncertain significance |
Showing 100 of 133 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.