GAS2L2

growth arrest specific 2 like 2

Summary

The protein encoded by this gene appears to crosslink microtubules and microfilaments and may be part of the cytoskeleton. This gene is mainly expressed in skeletal muscle. [provided by RefSeq, Jul 2011]

Known Variants123 total

rsidPosition (GRCh37)AllelesClassClinVar
rs382640317:34,071,647C/T—benign
rs11210952117:34,071,852T/A—benign
rs14820168117:34,071,917G/A—uncertain significance
rs11556876317:34,071,925G/A—benign
rs14591868617:34,071,968C/T—benign
rs5638670617:34,072,031A/G—benign
rs250991509617:34,072,035T/C—likely benign
rs250991509717:34,072,037C/G—uncertain significance
rs78247186717:34,072,045C/T—uncertain significance
rs7521507517:34,072,074C/T—benign
rs14938278117:34,072,083G/A—likely benign
rs78240083017:34,072,088G/A—uncertain significance
rs14472076717:34,072,174C/T—uncertain significance
rs78195353917:34,072,175G/A—uncertain significance
rs14851691817:34,072,210G/A—uncertain significance
rs58767503217:34,072,228C/T—likely benign
rs11466419817:34,072,245C/T—benign
rs14527397617:34,072,276T/C—likely benign
rs58760056317:34,072,309G/A—conflicting classifications of pathogenicity
rs115821622817:34,072,355G/T—uncertain significance
rs7815725417:34,072,386A/G—likely benign
rs37066426517:34,072,394T/C—uncertain significance
rs155559872817:34,072,396G/C—uncertain significance
rs119693904817:34,072,501G/A—uncertain significance
rs13786097717:34,072,519A/G—benign
rs14150099717:34,072,529G/A—uncertain significance
rs374437417:34,072,555A/G—benign
rs102411254217:34,072,633C/T—uncertain significance
rs78219174617:34,072,643T/C—uncertain significance
rs14618732317:34,072,736C/T—conflicting classifications of pathogenicity
rs250991612517:34,072,739C/A—uncertain significance
rs135395740917:34,072,759C/T—likely benign
rs117134666117:34,072,790A/G—likely benign
rs155559882717:34,072,794C/A—uncertain significance
rs250991623417:34,072,809C/T—uncertain significance
rs116763638017:34,072,814C/G—likely benign
rs58772327617:34,072,836C/G—uncertain significance
rs78239632017:34,072,865C/T—uncertain significance
rs14724752317:34,072,867T/C—likely benign
rs78209486117:34,072,868G/A—uncertain significance
rs14264169317:34,072,872G/A—likely benign
rs14531306217:34,072,895C/T—uncertain significance
rs14412834217:34,072,896G/A—likely benign
rs1260259017:34,072,898C/T—benign
rs78265712917:34,072,912G/T—uncertain significance
rs78248417817:34,072,913G/C—uncertain significance
rs15118348217:34,072,914G/C—uncertain significance
rs155559886517:34,072,921C/T—likely benign
rs131751776317:34,072,932C/A—uncertain significance
rs250991639417:34,072,946T/C—uncertain significance
rs14029388117:34,072,958G/A—uncertain significance
rs14402455217:34,072,984C/A—uncertain significance
rs19992191017:34,072,985G/A—uncertain significance
rs14077616417:34,073,004G/A—likely benign
rs18584640317:34,073,042G/A—likely benign
rs20224523917:34,073,053G/C—uncertain significance
rs13844317317:34,073,074G/A—uncertain significance
rs14392132317:34,073,075C/T—uncertain significance
rs14299203317:34,073,093G/A—uncertain significance
rs13962479317:34,073,120C/T—benign
rs8003398117:34,073,138G/A—benign
rs148274464217:34,073,165A/T—uncertain significance
rs20015205417:34,073,166T/C—uncertain significance
rs78248512317:34,073,176G/C—uncertain significance
rs155559893817:34,073,188A/G—uncertain significance
rs13927732917:34,073,194C/T—likely benign
rs11595557217:34,073,219C/T—likely benign
rs20210027217:34,073,225C/T—uncertain significance
rs7560895117:34,073,226G/A—likely benign
rs58770243917:34,073,252G/A—uncertain significance
rs5613570317:34,073,301T/C—benign
rs13914164617:34,073,320G/A—likely benign
rs250991682417:34,073,327A/C—uncertain significance
rs78253928217:34,073,347T/C—uncertain significance
rs14936530517:34,073,391C/T—likely benign
rs78179299117:34,073,402A/G—likely benign
rs7399029617:34,073,403A/G—benign
rs78249383717:34,074,042A/T—uncertain significance
rs20000314417:34,074,063C/A—likely benign
rs123204257017:34,074,065C/T—uncertain significance
rs19981449417:34,074,068G/A—uncertain significance
rs15079251917:34,074,089C/T—likely benign
rs78225237817:34,074,114G/A—uncertain significance
rs78262523817:34,074,158A/G—likely benign
rs20178241017:34,074,182C/T—uncertain significance
rs14598364517:34,074,252G/A—uncertain significance
rs155559915017:34,074,279G/A—uncertain significance
rs78262421017:34,074,894T/C—uncertain significance
rs155559925117:34,074,896T/C—likely benign
rs78242859717:34,074,928C/T—uncertain significance
rs14258624717:34,074,929G/A—likely benign
rs20219242417:34,074,940G/A—uncertain significance
rs58762783217:34,074,958G/A—uncertain significance
rs11411952317:34,075,129A/G—benign
rs78212108817:34,076,208C/T—uncertain significance
rs14050642417:34,076,211G/A—likely benign
rs37064688717:34,077,100T/C—uncertain significance
rs78235204617:34,077,137G/T—uncertain significance
rs91935648917:34,077,199A/G—uncertain significance
rs147066188217:34,077,203C/T—uncertain significance

Showing 100 of 123 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.