THSD7B

thrombospondin type 1 domain containing 7B

Summary

Predicted to be involved in actin cytoskeleton organization. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants103 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs10205354	2:137,549,884	A/G	intron variant	—
rs1427593	2:137,555,224	T/G	—	—
rs13026471	2:137,564,022	C/T	intron variant	—
rs34399632	2:137,571,174	A/G	intron variant	—
rs35009137	2:137,576,157	A/G	intron variant	—
rs11688567	2:137,581,062	T/G	intron variant	—
rs13002862	2:137,613,935	C/A	intron variant	—
rs1346732	2:137,621,703	T/G	—	—
rs957852183	2:137,748,499	A/G	—	likely benign
rs979976	2:137,768,702	A/T	—	—
rs775249555	2:137,814,025	G/A	—	uncertain significance
rs2467741377	2:137,814,061	G/T	—	uncertain significance
rs747634114	2:137,814,172	G/A	—	uncertain significance
rs541618030	2:137,814,214	G/A	—	uncertain significance
rs758191211	2:137,814,226	C/G	—	uncertain significance
rs575304657	2:137,814,239	A/G	—	uncertain significance
rs1055818319	2:137,814,388	T/A	—	uncertain significance
rs746159470	2:137,814,710	A/G	—	uncertain significance
rs200250890	2:137,814,719	C/T	—	uncertain significance
rs550601759	2:137,852,540	A/G	—	uncertain significance
rs369577932	2:137,852,588	C/T	—	uncertain significance
rs751622400	2:137,852,613	G/C	—	uncertain significance
rs369766346	2:137,852,624	G/A	—	uncertain significance
rs140063610	2:137,852,652	C/A	—	uncertain significance
rs758308510	2:137,852,667	G/A	—	uncertain significance
rs767523442	2:137,872,774	C/T	—	uncertain significance
rs892877	2:137,873,347	A/G	intron variant	—
rs1469622	2:137,875,875	T/C	regulatory region variant	—
rs116067048	2:137,898,642	C/G	intron variant	—
rs569237144	2:137,917,821	G/A	—	uncertain significance
rs200929460	2:137,917,846	A/T	—	uncertain significance
rs781503094	2:137,917,861	C/T	—	uncertain significance
rs561914228	2:137,928,328	C/T	—	uncertain significance
rs375376843	2:137,928,379	G/A	—	uncertain significance
rs778330063	2:137,928,490	G/A	—	uncertain significance
rs61742399	2:137,928,500	A/G	—	uncertain significance
rs1427578911	2:137,988,688	A/T	—	uncertain significance
rs61741154	2:137,988,713	C/T	—	uncertain significance
rs775620697	2:137,988,757	G/A	—	uncertain significance
rs187887961	2:137,990,472	G/A	—	uncertain significance
rs755824865	2:137,990,483	C/A	—	uncertain significance
rs1466022055	2:137,990,484	C/A	—	uncertain significance
rs779241674	2:137,990,498	C/T	—	uncertain significance
rs1681679554	2:137,990,645	A/G	—	uncertain significance
rs763566457	2:137,990,681	G/T	—	uncertain significance
rs764826188	2:137,990,684	G/A	—	uncertain significance
rs373850259	2:138,000,053	C/T	—	uncertain significance
rs370266523	2:138,000,059	G/A	—	uncertain significance
rs2467514891	2:138,030,194	G/C	—	uncertain significance
rs2467519659	2:138,033,582	G/A	—	uncertain significance
rs13415724	2:138,077,603	T/C	intron variant	—
rs10496768	2:138,079,954	G/A	intron variant	—
rs13405020	2:138,142,164	G/T	—	—
rs200743398	2:138,163,324	C/T	—	uncertain significance
rs1403601993	2:138,163,339	A/G	—	uncertain significance
rs769449816	2:138,169,230	T/C	—	uncertain significance
rs369691977	2:138,169,251	G/C	—	uncertain significance
rs372661542	2:138,169,253	G/A	—	uncertain significance
rs544470059	2:138,169,326	G/T	—	uncertain significance
rs564630499	2:138,169,334	C/T	—	uncertain significance
rs1333848894	2:138,169,360	T/G	—	uncertain significance
rs764080822	2:138,169,374	G/A	—	uncertain significance
rs114389936	2:138,190,246	C/T	intron variant	—
rs770009363	2:138,208,484	G/A	—	uncertain significance
rs769221184	2:138,208,550	A/G	—	uncertain significance
rs1869324	2:138,227,442	G/A	intron variant	—
rs550849687	2:138,253,816	A/G	—	—
rs13382553	2:138,264,231	A/G	intron variant	—
rs2375518	2:138,270,224	G/C	—	—
rs532858227	2:138,317,634	G/C	—	—
rs13400612	2:138,318,976	C/G	intron variant	—
rs757748999	2:138,320,819	A/G	—	uncertain significance
rs1431031275	2:138,320,890	C/T	—	uncertain significance
rs139737002	2:138,329,996	G/A	—	uncertain significance
rs565607197	2:138,340,040	C/T	—	—
rs540882298	2:138,373,754	C/A	—	uncertain significance
rs2467391546	2:138,373,778	C/T	—	uncertain significance
rs1364553570	2:138,373,878	A/C	—	uncertain significance
rs148820327	2:138,373,879	T/A	—	uncertain significance
rs777398725	2:138,373,884	C/T	—	uncertain significance
rs1038006201	2:138,375,986	A/C	—	uncertain significance
rs764914187	2:138,375,991	G/A	—	uncertain significance
rs377484305	2:138,376,009	G/A	—	uncertain significance
rs371445184	2:138,376,018	C/T	—	uncertain significance
rs781272734	2:138,376,028	G/A	—	uncertain significance
rs2467397045	2:138,376,067	A/G	—	uncertain significance
rs352181	2:138,376,538	C/A	intron variant	—
rs370520413	2:138,378,230	G/A	—	uncertain significance
rs747898935	2:138,400,070	G/A	—	uncertain significance
rs745747984	2:138,400,109	G/A	—	uncertain significance
rs16839236	2:138,404,751	G/A	intron variant	—
rs757187488	2:138,413,072	G/A	—	uncertain significance
rs1298491315	2:138,413,124	C/G	—	uncertain significance
rs377158080	2:138,413,147	C/A	—	uncertain significance
rs375009416	2:138,414,449	C/T	—	uncertain significance
rs760657010	2:138,414,656	C/T	—	uncertain significance
rs1192284371	2:138,414,680	A/G	—	uncertain significance
rs2104817816	2:138,414,713	A/C	—	uncertain significance
rs147732921	2:138,414,718	G/A	—	likely benign
rs368781810	2:138,417,269	C/T	—	uncertain significance

Showing 100 of 103 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.