SPP2

secreted phosphoprotein 2

Summary

This gene encodes a secreted phosphoprotein that is a member of the cystatin superfamily. [provided by RefSeq, Oct 2008]

Known Variants160 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs143244045	2:234,959,430	C/A	—	likely benign
rs907542594	2:234,959,440	A/C	—	likely benign
rs145529777	2:234,959,456	C/T	—	conflicting classifications of pathogenicity
rs142534488	2:234,959,457	G/T	—	likely benign
rs756261230	2:234,959,459	T/C	—	uncertain significance
rs374261845	2:234,959,478	T/C	—	likely benign
rs1490945405	2:234,959,480	T/C	—	uncertain significance
rs2470229677	2:234,959,489	T/A	—	uncertain significance
rs369178666	2:234,959,494	A/G	—	uncertain significance
rs1315920333	2:234,959,499	C/T	—	likely benign
rs773241018	2:234,959,502	C/T	—	likely benign
rs1209574905	2:234,959,505	G/C	—	uncertain significance
rs760561082	2:234,959,510	G/A	—	uncertain significance
rs1299915925	2:234,959,535	G/A	—	likely benign
rs200433915	2:234,959,601	G/C	—	likely benign
rs202019698	2:234,959,606	C/A	—	uncertain significance
rs377665604	2:234,959,607	G/A	—	likely benign
rs1693479406	2:234,959,610	T/C	—	likely benign
rs1400560316	2:234,959,614	G/T	—	uncertain significance
rs1377115981	2:234,959,624	T/C	—	uncertain significance
rs1693479793	2:234,959,625	G/T	—	likely benign
rs753888543	2:234,959,634	C/T	—	likely benign
rs755087069	2:234,959,635	G/A	—	uncertain significance
rs115788299	2:234,959,637	T/C	—	likely benign
rs758562666	2:234,959,641	T/G	—	uncertain significance
rs34347825	2:234,959,642	C/T	—	likely benign
rs200706917	2:234,959,649	A/C	—	uncertain significance
rs138848923	2:234,959,652	G/A	—	likely benign
rs114861790	2:234,959,653	G/A	—	uncertain significance
rs768201739	2:234,959,655	T/A	—	conflicting classifications of pathogenicity
rs2125447533	2:234,959,673	G/A	—	likely benign
rs1693482369	2:234,959,683	A/T	—	uncertain significance
rs760990067	2:234,959,684	A/T	—	uncertain significance
rs144683165	2:234,959,687	C/G	—	uncertain significance
rs551029738	2:234,959,689	C/T	—	uncertain significance
rs202033706	2:234,959,694	A/G	—	likely benign
rs143082886	2:234,959,702	C/T	—	conflicting classifications of pathogenicity
rs150764101	2:234,959,703	G/T	—	likely benign
rs758641331	2:234,959,707	C/G	—	benign
rs150743830	2:234,959,709	G/C	—	likely benign
rs1693483701	2:234,959,712	T/C	—	likely benign
rs200722650	2:234,959,713	C/T	—	uncertain significance
rs757044100	2:234,959,714	G/A	—	uncertain significance
rs781164889	2:234,959,715	G/C	—	likely benign
rs2125447672	2:234,959,716	G/A	—	uncertain significance
rs2470230790	2:234,959,722	A/G	—	uncertain significance
rs953292820	2:234,959,740	G/A	—	uncertain significance
rs779648916	2:234,959,741	T/G	—	uncertain significance
rs748819179	2:234,959,746	G/T	—	likely benign
rs1367454281	2:234,959,752	T/G	—	likely benign
rs2470230920	2:234,959,756	A/G	—	likely benign
rs1507516	2:234,960,570	C/A	intron variant	—
rs1246989227	2:234,967,460	G/A	—	likely benign
rs192368772	2:234,967,462	A/C	—	likely benign
rs1467399974	2:234,967,464	C/A	—	likely benign
rs767366023	2:234,967,481	T/C	—	conflicting classifications of pathogenicity
rs371778962	2:234,967,498	A/T	—	uncertain significance
rs1300520957	2:234,967,501	A/G	—	uncertain significance
rs149868175	2:234,967,531	C/T	—	uncertain significance
rs746289744	2:234,967,532	G/A	—	uncertain significance
rs593668	2:234,967,539	A/T	—	benign
rs1261837202	2:234,967,542	A/G	—	likely benign
rs763549452	2:234,967,543	T/C	—	conflicting classifications of pathogenicity
rs1167352947	2:234,967,544	G/A	—	uncertain significance
rs1399954776	2:234,967,546	A/G	—	uncertain significance
rs2125455747	2:234,967,547	G/A	—	conflicting classifications of pathogenicity
rs1297018807	2:234,967,548	G/C	—	uncertain significance
rs1293713918	2:234,967,564	G/T	—	uncertain significance
rs1693662893	2:234,967,565	A/G	—	uncertain significance
rs76941072	2:234,967,569	C/T	—	benign
rs74975266	2:234,967,570	G/A	—	uncertain significance
rs200097563	2:234,967,597	T/G	—	uncertain significance
rs1419597275	2:234,967,603	G/C	—	uncertain significance
rs2470247626	2:234,967,613	G/A	—	likely benign
rs369576943	2:234,967,614	G/A	—	likely benign
rs746200177	2:234,967,618	C/T	—	likely benign
rs757943898	2:234,968,993	C/T	—	likely benign
rs1027608262	2:234,968,995	C/T	—	likely benign
rs952488913	2:234,969,014	C/T	—	uncertain significance
rs780218526	2:234,969,017	C/T	—	uncertain significance
rs749731859	2:234,969,018	A/G	—	likely benign
rs2125457347	2:234,969,019	G/C	—	uncertain significance
rs1213169901	2:234,969,022	G/C	—	uncertain significance
rs779526667	2:234,969,036	C/T	—	likely benign
rs141839502	2:234,969,037	G/A	—	uncertain significance
rs1198857202	2:234,969,045	A/G	—	likely benign
rs1693694720	2:234,969,050	C/T	—	uncertain significance
rs2470251041	2:234,969,051	C/T	—	likely benign
rs1015197391	2:234,969,052	C/T	—	uncertain significance
rs772225535	2:234,969,053	A/C	—	uncertain significance
rs199501024	2:234,969,058	G/A	—	uncertain significance
rs1693695066	2:234,969,061	C/T	—	uncertain significance
rs1693695123	2:234,969,062	A/G	—	uncertain significance
rs150700652	2:234,969,066	C/T	—	likely benign
rs202217477	2:234,969,067	G/A	—	uncertain significance
rs575965941	2:234,969,076	C/T	—	uncertain significance
rs376262894	2:234,969,077	G/C	—	uncertain significance
rs150395122	2:234,969,082	A/T	—	uncertain significance
rs200554838	2:234,969,087	G/T	—	uncertain significance
rs768729113	2:234,969,089	C/T	—	uncertain significance

Showing 100 of 160 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.