ZNF292

zinc finger protein 292

Summary

This gene encodes a growth hormone-dependent, zinc finger transcription factor that functions as a tumor suppressor. Naturally occurring mutations in this gene are associated with gastric cancer, colorectal cancer, and chronic lymphocytic leukemia. [provided by RefSeq, May 2017]

Known Variants407 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2481824518	6:87,865,311	T/G	—	uncertain significance
rs891555279	6:87,865,328	G/A	—	uncertain significance
rs1770498812	6:87,865,348	C/T	—	likely benign
rs749712579	6:87,865,349	G/A	—	uncertain significance
rs554384428	6:87,865,356	G/C	—	uncertain significance
rs370959721	6:87,865,357	C/A	—	likely benign
rs373333120	6:87,865,367	G/A	—	likely benign
rs1770500301	6:87,865,370	G/C	—	likely pathogenic
rs201296869	6:87,865,377	A/C	—	likely benign
rs2481824976	6:87,865,388	G/C	—	uncertain significance
rs1018215636	6:87,865,391	C/T	—	uncertain significance
rs973945684	6:87,865,427	C/T	—	uncertain significance
rs1925690	6:87,867,063	T/A	—	—
rs9344685	6:87,874,662	G/A	—	—
rs9444480	6:87,879,376	T/C	downstream gene variant	—
rs7757330	6:87,886,335	A/G	upstream gene variant	—
rs6454593	6:87,904,899	G/A	intron variant	—
rs1772730013	6:87,925,627	C/G	—	uncertain significance
rs1216473967	6:87,925,636	G/A	—	uncertain significance
rs2482017974	6:87,925,641	G/C	—	uncertain significance
rs865909396	6:87,925,717	C/T	—	pathogenic
rs1327633366	6:87,925,721	C/G	—	uncertain significance
rs377546821	6:87,925,746	T/G	—	uncertain significance
rs2482019166	6:87,925,776	G/A	—	uncertain significance
rs2108268	6:87,925,826	G/C	—	—
rs2127803038	6:87,926,045	C/T	—	uncertain significance
rs2482036069	6:87,928,317	G/A	—	uncertain significance
rs1386023402	6:87,928,318	C/T	—	uncertain significance
rs2482036334	6:87,928,347	T/G	—	uncertain significance
rs2482036628	6:87,928,374	G/A	—	uncertain significance
rs1582439939	6:87,928,390	T/C	—	uncertain significance
rs758351988	6:87,928,413	A/T	—	likely benign
rs746738863	6:87,928,416	A/G	—	uncertain significance
rs375133485	6:87,928,426	A/G	—	likely benign
rs2482124878	6:87,943,087	A/G	—	uncertain significance
rs1446051059	6:87,943,104	C/G	—	uncertain significance
rs2482126121	6:87,943,226	A/G	—	uncertain significance
rs2482126391	6:87,943,250	G/A	—	uncertain significance
rs2482207163	6:87,953,190	T/G	—	likely pathogenic
rs749873195	6:87,953,248	A/G	—	likely benign
rs1774419692	6:87,953,265	G/A	—	conflicting classifications of pathogenicity
rs2127840543	6:87,953,269	T/C	—	likely pathogenic
rs2482208154	6:87,953,275	T/C	—	uncertain significance
rs781382344	6:87,953,285	G/A	—	likely benign
rs770128233	6:87,953,317	T/C	—	uncertain significance
rs867732475	6:87,953,321	C/A	—	likely pathogenic
rs184839913	6:87,953,322	T/G	—	likely benign
rs546063923	6:87,955,294	C/T	—	uncertain significance
rs368623280	6:87,955,299	A/G	—	likely benign
rs748403929	6:87,955,306	T/G	—	likely benign
rs2482282924	6:87,964,365	C/T	—	uncertain significance
rs2482283134	6:87,964,381	G/C	—	uncertain significance
rs976963327	6:87,964,413	G/A	—	uncertain significance
rs2482283894	6:87,964,449	A/G	—	uncertain significance
rs759209377	6:87,964,486	C/T	—	uncertain significance
rs2482284460	6:87,964,507	G/A	—	uncertain significance
rs957020155	6:87,964,525	A/T	—	uncertain significance
rs760272408	6:87,964,537	A/G	—	uncertain significance
rs116277830	6:87,964,553	G/A	—	likely benign
rs75154406	6:87,964,574	G/A	—	likely benign
rs1195660356	6:87,964,606	A/G	—	uncertain significance
rs749274149	6:87,964,609	A/G	—	uncertain significance
rs1775128550	6:87,964,617	A/G	—	uncertain significance
rs2127856543	6:87,964,620	C/T	—	uncertain significance
rs376610075	6:87,964,634	C/T	—	likely benign
rs1215967523	6:87,964,707	C/T	—	conflicting classifications of pathogenicity
rs1775133764	6:87,964,735	A/C	—	uncertain significance
rs1166797338	6:87,964,755	A/G	—	conflicting classifications of pathogenicity
rs2482287354	6:87,964,761	G/T	—	pathogenic
rs2127857000	6:87,964,770	G/C	—	uncertain significance
rs1457087238	6:87,964,771	A/G	—	uncertain significance
rs1005599952	6:87,964,831	A/G	—	uncertain significance
rs76287062	6:87,964,846	G/T	—	benign
rs2482288671	6:87,964,858	A/G	—	uncertain significance
rs1775143865	6:87,964,914	C/T	—	likely pathogenic
rs2482289812	6:87,964,965	T/C	—	uncertain significance
rs182042752	6:87,964,973	G/A	—	likely benign
rs370886893	6:87,964,994	A/G	—	uncertain significance
rs373131243	6:87,965,019	C/T	—	likely pathogenic
rs2482290215	6:87,965,020	G/A	—	uncertain significance
rs2127857888	6:87,965,062	C/T	—	uncertain significance
rs1248728289	6:87,965,079	T/C	—	uncertain significance
rs2127858055	6:87,965,107	A/C	—	uncertain significance
rs1280021381	6:87,965,179	G/C	—	uncertain significance
rs1775159559	6:87,965,205	G/T	—	uncertain significance
rs1775161294	6:87,965,244	C/T	—	likely pathogenic
rs1160342281	6:87,965,293	A/G	—	uncertain significance
rs1775170046	6:87,965,358	C/G	—	uncertain significance
rs752579678	6:87,965,370	C/T	—	likely benign
rs373848653	6:87,965,399	T/C	—	likely benign
rs200991861	6:87,965,406	T/A	—	uncertain significance
rs2482295867	6:87,965,430	T/C	—	uncertain significance
rs1775175416	6:87,965,451	G/A	—	uncertain significance
rs375509766	6:87,965,459	G/A	—	likely benign
rs767558967	6:87,965,496	A/T	—	uncertain significance
rs41273271	6:87,965,519	C/T	—	benign
rs753507047	6:87,965,525	C/T	—	likely benign
rs6908834	6:87,965,528	T/C	—	benign
rs2482297353	6:87,965,551	C/A	—	uncertain significance
rs770183170	6:87,965,605	T/C	—	likely benign

Showing 100 of 407 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.