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

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1850744	4:9,790,712	T/C	downstream gene variant	—
rs35582635	4:9,816,409	G/A	intron variant	—
rs938557	4:9,827,556	T/C	downstream gene variant	—
rs1188213874	4:9,827,885	T/C	—	uncertain significance
rs550035001	4:9,827,892	G/T	—	uncertain significance
rs144294717	4:9,827,911	C/A	—	benign
rs886059751	4:9,827,973	G/C	—	uncertain significance
rs1725133187	4:9,828,017	C/T	—	uncertain significance
rs1725134551	4:9,828,022	T/C	—	uncertain significance
rs755671863	4:9,828,026	G/C	—	uncertain significance
rs146590565	4:9,828,045	A/G	—	benign
rs779863644	4:9,828,063	G/A	—	uncertain significance
rs2545745885	4:9,828,069	C/G	—	uncertain significance
rs144428359	4:9,828,099	G/A	—	likely benign
rs899553019	4:9,828,124	T/G	—	uncertain significance
rs771866622	4:9,828,126	G/C	—	conflicting classifications of pathogenicity
rs1445138560	4:9,828,133	T/A	—	uncertain significance
rs763124804	4:9,828,178	A/G	—	benign
rs752093635	4:9,828,185	T/C	—	uncertain significance
rs1259250257	4:9,828,206	A/G	—	uncertain significance
rs371746690	4:9,828,230	G/A	—	likely benign
rs139913518	4:9,828,391	G/A	—	likely benign
rs4697895	4:9,828,484	T/C	—	benign
rs73223788	4:9,828,502	T/C	—	benign
rs185961732	4:9,831,056	G/C	intron variant	—
rs12642114	4:9,836,190	A/G	—	benign
rs3775950	4:9,836,366	T/C	—	benign
rs930099562	4:9,836,504	C/T	—	uncertain significance
rs745845092	4:9,836,511	G/T	—	uncertain significance
rs779780913	4:9,836,525	G/T	—	uncertain significance
rs886059752	4:9,836,532	A/G	—	uncertain significance
rs1476209699	4:9,836,534	C/A	—	uncertain significance
rs1726778228	4:9,836,538	G/C	—	uncertain significance
rs748271861	4:9,836,539	T/C	—	uncertain significance
rs772321208	4:9,836,541	G/A	—	likely benign
rs200305429	4:9,836,555	C/T	—	uncertain significance
rs375423927	4:9,836,556	G/A	—	likely benign
rs762605826	4:9,836,568	G/A	—	uncertain significance
rs368484282	4:9,836,580	C/T	—	likely benign
rs372201423	4:9,836,581	G/A	—	likely pathogenic
rs544017062	4:9,836,585	G/A	—	uncertain significance
rs2545816901	4:9,836,609	C/T	—	uncertain significance
rs556085300	4:9,836,622	C/T	—	likely benign
rs147534794	4:9,836,625	G/A	—	likely benign
rs372628073	4:9,836,638	G/A	—	likely benign
rs7665666	4:9,836,861	T/A	—	benign
rs575029746	4:9,846,660	C/G	—	—
rs56288911	4:9,865,615	T/C	intron variant	—
rs9684002	4:9,866,498	G/A	intron variant	—
rs1568318	4:9,871,541	T/C	intron variant	—
rs534867559	4:9,883,181	T/C	—	—
rs4697904	4:9,888,994	C/T	—	benign
rs4697905	4:9,889,042	T/C	—	benign
rs6836878	4:9,889,069	C/T	—	benign
rs1393248566	4:9,889,175	G/T	—	likely benign
rs747079268	4:9,889,182	G/A	—	likely benign
rs747922850	4:9,889,185	C/T	—	uncertain significance
rs2546255030	4:9,889,227	T/C	—	uncertain significance
rs386352361	4:9,889,242	G/A	—	uncertain significance
rs121908323	4:9,889,247	G/C	missense variant	pathogenic
rs369754879	4:9,889,261	G/A	—	likely benign
rs6818572	4:9,889,448	G/A	—	benign
rs56399359	4:9,889,487	G/A	—	benign
rs4697906	4:9,889,896	C/T	—	—
rs28489733	4:9,892,061	C/A	—	benign
rs10939602	4:9,892,102	T/C	—	benign
rs28571073	4:9,892,139	A/G	—	likely benign
rs187946156	4:9,892,226	C/T	—	benign
rs780348287	4:9,892,227	G/A	—	likely benign
rs1737202797	4:9,892,230	T/C	—	uncertain significance
rs191072192	4:9,892,246	C/T	—	benign
rs1271040335	4:9,892,252	G/C	—	likely benign
rs1737213093	4:9,892,265	A/G	—	uncertain significance
rs1183123584	4:9,892,276	C/T	—	uncertain significance
rs751716406	4:9,892,297	G/A	—	likely benign
rs145536778	4:9,892,310	C/T	—	uncertain significance
rs121908321	4:9,892,311	G/A	missense variant	pathogenic
rs755325843	4:9,892,325	A/G	—	uncertain significance
rs1447625985	4:9,892,336	C/G	—	uncertain significance
rs182359903	4:9,892,354	G/A	—	likely benign
rs114361719	4:9,892,424	C/G	—	likely benign
rs80204783	4:9,894,371	C/T	intron variant	—
rs144499258	4:9,902,580	A/C	intron variant	—
rs2280203	4:9,909,559	G/T	—	benign
rs753123621	4:9,909,843	C/T	—	likely benign
rs2280204	4:9,909,850	T/G	—	benign
rs560972980	4:9,909,867	C/T	—	uncertain significance
rs1362435704	4:9,909,880	C/G	—	uncertain significance
rs367692082	4:9,909,887	C/T	—	uncertain significance
rs760956353	4:9,909,907	G/A	—	likely benign
rs267600301	4:9,909,913	G/C	—	uncertain significance
rs576420234	4:9,909,922	C/T	—	benign
rs2280205	4:9,909,923	G/A	—	benign
rs116742917	4:9,909,926	G/A	—	benign
rs748838061	4:9,909,968	A/G	—	uncertain significance
rs6825187	4:9,915,325	T/C	intron variant	—
rs11722228	4:9,915,741	C/T	intron variant	—
rs6823877	4:9,921,931	T/C	—	benign
rs765285398	4:9,921,992	C/T	—	likely benign
rs753237840	4:9,921,993	G/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.