SLC2A9

solute carrier family 2 member 9

Summary

This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

Known Variants337 total

rsidPosition (GRCh37)AllelesClassClinVar
rs18507444:9,790,712T/Cdownstream gene variant—
rs355826354:9,816,409G/Aintron variant—
rs9385574:9,827,556T/Cdownstream gene variant—
rs11882138744:9,827,885T/C—uncertain significance
rs5500350014:9,827,892G/T—uncertain significance
rs1442947174:9,827,911C/A—benign
rs8860597514:9,827,973G/C—uncertain significance
rs17251331874:9,828,017C/T—uncertain significance
rs17251345514:9,828,022T/C—uncertain significance
rs7556718634:9,828,026G/C—uncertain significance
rs1465905654:9,828,045A/G—benign
rs7798636444:9,828,063G/A—uncertain significance
rs25457458854:9,828,069C/G—uncertain significance
rs1444283594:9,828,099G/A—likely benign
rs8995530194:9,828,124T/G—uncertain significance
rs7718666224:9,828,126G/C—conflicting classifications of pathogenicity
rs14451385604:9,828,133T/A—uncertain significance
rs7631248044:9,828,178A/G—benign
rs7520936354:9,828,185T/C—uncertain significance
rs12592502574:9,828,206A/G—uncertain significance
rs3717466904:9,828,230G/A—likely benign
rs1399135184:9,828,391G/A—likely benign
rs46978954:9,828,484T/C—benign
rs732237884:9,828,502T/C—benign
rs1859617324:9,831,056G/Cintron variant—
rs126421144:9,836,190A/G—benign
rs37759504:9,836,366T/C—benign
rs9300995624:9,836,504C/T—uncertain significance
rs7458450924:9,836,511G/T—uncertain significance
rs7797809134:9,836,525G/T—uncertain significance
rs8860597524:9,836,532A/G—uncertain significance
rs14762096994:9,836,534C/A—uncertain significance
rs17267782284:9,836,538G/C—uncertain significance
rs7482718614:9,836,539T/C—uncertain significance
rs7723212084:9,836,541G/A—likely benign
rs2003054294:9,836,555C/T—uncertain significance
rs3754239274:9,836,556G/A—likely benign
rs7626058264:9,836,568G/A—uncertain significance
rs3684842824:9,836,580C/T—likely benign
rs3722014234:9,836,581G/A—likely pathogenic
rs5440170624:9,836,585G/A—uncertain significance
rs25458169014:9,836,609C/T—uncertain significance
rs5560853004:9,836,622C/T—likely benign
rs1475347944:9,836,625G/A—likely benign
rs3726280734:9,836,638G/A—likely benign
rs76656664:9,836,861T/A—benign
rs5750297464:9,846,660C/G——
rs562889114:9,865,615T/Cintron variant—
rs96840024:9,866,498G/Aintron variant—
rs15683184:9,871,541T/Cintron variant—
rs5348675594:9,883,181T/C——
rs46979044:9,888,994C/T—benign
rs46979054:9,889,042T/C—benign
rs68368784:9,889,069C/T—benign
rs13932485664:9,889,175G/T—likely benign
rs7470792684:9,889,182G/A—likely benign
rs7479228504:9,889,185C/T—uncertain significance
rs25462550304:9,889,227T/C—uncertain significance
rs3863523614:9,889,242G/A—uncertain significance
rs1219083234:9,889,247G/Cmissense variantpathogenic
rs3697548794:9,889,261G/A—likely benign
rs68185724:9,889,448G/A—benign
rs563993594:9,889,487G/A—benign
rs46979064:9,889,896C/T——
rs284897334:9,892,061C/A—benign
rs109396024:9,892,102T/C—benign
rs285710734:9,892,139A/G—likely benign
rs1879461564:9,892,226C/T—benign
rs7803482874:9,892,227G/A—likely benign
rs17372027974:9,892,230T/C—uncertain significance
rs1910721924:9,892,246C/T—benign
rs12710403354:9,892,252G/C—likely benign
rs17372130934:9,892,265A/G—uncertain significance
rs11831235844:9,892,276C/T—uncertain significance
rs7517164064:9,892,297G/A—likely benign
rs1455367784:9,892,310C/T—uncertain significance
rs1219083214:9,892,311G/Amissense variantpathogenic
rs7553258434:9,892,325A/G—uncertain significance
rs14476259854:9,892,336C/G—uncertain significance
rs1823599034:9,892,354G/A—likely benign
rs1143617194:9,892,424C/G—likely benign
rs802047834:9,894,371C/Tintron variant—
rs1444992584:9,902,580A/Cintron variant—
rs22802034:9,909,559G/T—benign
rs7531236214:9,909,843C/T—likely benign
rs22802044:9,909,850T/G—benign
rs5609729804:9,909,867C/T—uncertain significance
rs13624357044:9,909,880C/G—uncertain significance
rs3676920824:9,909,887C/T—uncertain significance
rs7609563534:9,909,907G/A—likely benign
rs2676003014:9,909,913G/C—uncertain significance
rs5764202344:9,909,922C/T—benign
rs22802054:9,909,923G/A—benign
rs1167429174:9,909,926G/A—benign
rs7488380614:9,909,968A/G—uncertain significance
rs68251874:9,915,325T/Cintron variant—
rs117222284:9,915,741C/Tintron variant—
rs68238774:9,921,931T/C—benign
rs7652853984:9,921,992C/T—likely benign
rs7532378404:9,921,993G/A—likely benign

Showing 100 of 337 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.