LMO7

LIM domain 7

Summary

This gene encodes a protein containing a calponin homology (CH) domain, a PDZ domain, and a LIM domain, and may be involved in protein-protein interactions. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene, however, the full-length nature of some variants is not known. [provided by RefSeq, Jan 2009]

Known Variants135 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs140162071	13:76,195,882	A/G	—	uncertain significance
rs148440316	13:76,195,941	T/C	—	uncertain significance
rs369455674	13:76,195,965	G/C	—	uncertain significance
rs767168979	13:76,195,985	C/A	—	likely benign
rs1471520142	13:76,195,998	A/G	—	uncertain significance
rs750361918	13:76,197,410	T/C	—	uncertain significance
rs2138658985	13:76,197,445	A/T	—	uncertain significance
rs11841001	13:76,249,103	G/A	intron variant	—
rs9530458	13:76,249,275	T/A	—	—
rs9544020	13:76,253,247	A/T	—	—
rs111439095	13:76,254,433	A/G	intron variant	—
rs4884014	13:76,255,872	A/G	intron variant	—
rs9544022	13:76,257,266	G/C	intron variant	—
rs9544024	13:76,258,720	A/T	—	—
rs9573612	13:76,260,015	C/T	downstream gene variant	—
rs186102686	13:76,281,808	C/T	intron variant	—
rs1244575693	13:76,287,358	C/T	—	uncertain significance
rs2544545358	13:76,287,392	A/G	—	uncertain significance
rs140368500	13:76,301,190	G/A	—	likely benign
rs751118448	13:76,301,206	A/G	—	uncertain significance
rs769016460	13:76,301,218	C/T	—	uncertain significance
rs138203445	13:76,301,229	G/C	—	uncertain significance
rs539514	13:76,326,282	A/T	intron variant	—
rs474240	13:76,351,286	A/G	intron variant	—
rs41286124	13:76,374,870	C/T	—	likely benign
rs146713281	13:76,375,013	G/C	—	uncertain significance
rs75569760	13:76,378,447	G/A	—	benign
rs371465917	13:76,378,491	C/T	—	uncertain significance
rs375012849	13:76,378,506	C/T	—	uncertain significance
rs138809597	13:76,378,541	C/T	—	uncertain significance
rs368333382	13:76,378,601	A/G	—	uncertain significance
rs1299298884	13:76,379,643	G/A	—	uncertain significance
rs182275016	13:76,379,728	A/G	—	uncertain significance
rs779802011	13:76,379,763	A/C	—	uncertain significance
rs552675352	13:76,379,853	A/G	—	uncertain significance
rs368045003	13:76,381,617	C/A	—	uncertain significance
rs182908547	13:76,381,679	T/C	—	likely benign
rs2548688696	13:76,381,705	C/G	—	uncertain significance
rs200211735	13:76,381,719	C/T	—	uncertain significance
rs372308172	13:76,381,720	G/A	—	uncertain significance
rs539051277	13:76,381,727	G/T	—	uncertain significance
rs372735020	13:76,381,855	G/A	—	uncertain significance
rs369620389	13:76,381,924	G/T	—	uncertain significance
rs755801347	13:76,381,932	G/A	—	uncertain significance
rs1476261503	13:76,381,996	A/G	—	uncertain significance
rs761293278	13:76,382,014	C/G	—	uncertain significance
rs759826765	13:76,382,025	G/A	—	uncertain significance
rs142687160	13:76,382,029	G/A	—	benign
rs2585628	13:76,382,051	C/T	—	benign
rs2055771501	13:76,382,139	T/G	—	uncertain significance
rs770634635	13:76,382,164	G/A	—	uncertain significance
rs368850681	13:76,382,223	G/A	—	uncertain significance
rs375894473	13:76,382,289	C/T	—	uncertain significance
rs768883595	13:76,382,302	G/C	—	uncertain significance
rs138475106	13:76,383,310	G/T	—	uncertain significance
rs144129171	13:76,391,322	G/A	—	uncertain significance
rs370670178	13:76,395,368	G/A	—	likely benign
rs374230301	13:76,395,386	G/A	—	uncertain significance
rs7998249	13:76,395,443	G/A	—	uncertain significance
rs768549930	13:76,395,480	A/G	—	uncertain significance
rs200351536	13:76,395,486	A/G	—	uncertain significance
rs775970006	13:76,395,515	C/T	—	uncertain significance
rs2057560949	13:76,395,554	G/A	—	uncertain significance
rs376028694	13:76,395,563	C/A	—	uncertain significance
rs41286128	13:76,395,590	C/T	—	uncertain significance
rs753624038	13:76,395,591	G/A	—	likely benign
rs771439389	13:76,395,608	A/G	—	uncertain significance
rs377059336	13:76,395,650	C/T	—	uncertain significance
rs1007995149	13:76,395,705	C/T	—	uncertain significance
rs369032047	13:76,395,728	C/A	—	uncertain significance
rs140740070	13:76,397,693	T/A	—	benign
rs151245949	13:76,397,701	A/G	—	uncertain significance
rs142994139	13:76,397,710	A/G	—	benign
rs142550237	13:76,397,737	G/C	—	uncertain significance
rs2548885972	13:76,397,753	C/A	—	likely benign
rs545157703	13:76,397,764	G/T	—	uncertain significance
rs962289502	13:76,397,768	G/A	—	uncertain significance
rs147546485	13:76,397,771	C/T	—	conflicting classifications of pathogenicity
rs370412695	13:76,397,791	G/A	—	likely benign
rs1320246912	13:76,397,888	C/A	—	uncertain significance
rs143899312	13:76,397,953	A/G	—	uncertain significance
rs779977216	13:76,397,959	G/C	—	uncertain significance
rs200869696	13:76,397,962	T/C	—	uncertain significance
rs376307236	13:76,398,005	C/T	—	uncertain significance
rs372046266	13:76,407,229	G/A	—	uncertain significance
rs200991869	13:76,407,287	C/G	—	uncertain significance
rs745409800	13:76,407,293	T/C	—	uncertain significance
rs556560630	13:76,408,439	G/A	—	uncertain significance
rs201883792	13:76,408,445	A/C	—	uncertain significance
rs369234596	13:76,408,508	C/T	—	uncertain significance
rs772186829	13:76,409,396	C/T	—	uncertain significance
rs182631787	13:76,409,449	G/T	—	uncertain significance
rs564271731	13:76,409,467	C/G	—	uncertain significance
rs2549027084	13:76,410,585	A/T	—	uncertain significance
rs367627741	13:76,412,291	C/T	—	uncertain significance
rs2059282158	13:76,412,310	G/T	—	uncertain significance
rs763860269	13:76,414,557	C/T	—	uncertain significance
rs1269222296	13:76,414,558	G/T	—	uncertain significance
rs368955588	13:76,414,561	G/C	—	uncertain significance
rs534973931	13:76,414,569	G/C	—	likely benign

Showing 100 of 135 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.