ZNF536

zinc finger protein 536

Summary

The protein encoded by this gene is a highly conserved zinc finger protein. The encoded protein is most abundant in brain, where it negatively regulates neuronal differentiation. [provided by RefSeq, Sep 2015]

Known Variants103 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs6510073	19:30,756,075	A/C	intron variant	—
rs185430475	19:30,848,514	C/G	intron variant	—
rs6510155	19:30,857,196	G/A	intron variant	—
rs559068449	19:30,878,345	C/A	—	—
rs4805566	19:30,918,316	T/A	intron variant	—
rs187291090	19:30,934,479	G/A	—	uncertain significance
rs756153627	19:30,934,483	G/A	—	uncertain significance
rs375667945	19:30,934,513	C/T	—	uncertain significance
rs765563824	19:30,934,669	A/G	—	uncertain significance
rs201542417	19:30,934,689	G/C	—	uncertain significance
rs2148154995	19:30,934,722	G/A	—	uncertain significance
rs1742527349	19:30,934,723	C/A	—	uncertain significance
rs2148156059	19:30,934,742	G/C	—	likely benign
rs778595563	19:30,934,869	C/A	—	uncertain significance
rs1173469112	19:30,935,059	G/C	—	uncertain significance
rs1040675243	19:30,935,085	G/T	—	uncertain significance
rs2148179837	19:30,935,244	A/G	—	uncertain significance
rs976936167	19:30,935,272	T/G	—	uncertain significance
rs1243549683	19:30,935,467	G/A	—	uncertain significance
rs370088671	19:30,935,469	C/T	—	uncertain significance
rs2148189304	19:30,935,479	G/T	—	uncertain significance
rs774965623	19:30,935,484	G/T	—	uncertain significance
rs2052235651	19:30,935,709	C/T	—	uncertain significance
rs1233854909	19:30,935,767	G/T	—	uncertain significance
rs1225011334	19:30,935,781	T/C	—	uncertain significance
rs2148202590	19:30,935,797	A/G	—	uncertain significance
rs148834715	19:30,935,859	G/A	—	likely benign
rs61743191	19:30,935,909	C/T	—	benign
rs752138319	19:30,935,911	C/T	—	uncertain significance
rs138204939	19:30,935,927	C/G	—	uncertain significance
rs769939047	19:30,935,952	G/A	—	uncertain significance
rs1430300403	19:30,935,956	C/T	—	uncertain significance
rs767972699	19:30,935,979	G/A	—	uncertain significance
rs2148212030	19:30,936,021	G/T	—	uncertain significance
rs2148212776	19:30,936,040	G/A	—	uncertain significance
rs754516880	19:30,936,132	G/T	—	uncertain significance
rs372107821	19:30,936,159	C/T	—	uncertain significance
rs1254086563	19:30,936,238	G/T	—	uncertain significance
rs2148221127	19:30,936,253	C/T	—	uncertain significance
rs779003416	19:30,936,258	A/G	—	uncertain significance
rs769207359	19:30,936,321	T/G	—	uncertain significance
rs2517501783	19:30,936,408	G/T	—	uncertain significance
rs149326839	19:30,936,431	G/A	—	likely benign
rs1233903961	19:30,936,462	C/T	—	uncertain significance
rs909932455	19:30,936,517	T/C	—	uncertain significance
rs149363496	19:30,936,554	C/T	—	benign
rs544804864	19:30,936,560	G/C	—	uncertain significance
rs969251122	19:30,936,567	G/T	—	uncertain significance
rs33428	19:30,937,843	A/G	intron variant	—
rs33436	19:30,943,677	A/G	intron variant	—
rs3786800	19:30,990,700	T/C	intron variant	—
rs73022871	19:30,990,705	C/A	—	—
rs55655041	19:30,995,200	T/A	—	—
rs11668301	19:31,016,196	A/G	intron variant	—
rs73026723	19:31,017,177	C/T	intron variant	—
rs11084553	19:31,019,780	A/G	intron variant	—
rs117798694	19:31,025,747	G/A	—	likely benign
rs755382445	19:31,025,756	A/G	—	uncertain significance
rs376861690	19:31,025,784	G/C	—	uncertain significance
rs375973209	19:31,025,786	G/A	—	uncertain significance
rs144474545	19:31,025,799	C/T	—	uncertain significance
rs114150736	19:31,025,845	G/A	—	benign
rs11666918	19:31,034,674	G/A	intron variant	—
rs12460433	19:31,035,649	C/A	intron variant	—
rs10418356	19:31,035,686	C/G	intron variant	—
rs2045618139	19:31,038,861	T/C	—	uncertain significance
rs142398595	19:31,038,947	C/T	—	likely benign
rs768923292	19:31,039,010	A/C	—	uncertain significance
rs143550497	19:31,039,257	G/A	—	likely benign
rs2045637020	19:31,039,260	G/C	—	uncertain significance
rs61741995	19:31,039,357	C/A	—	benign
rs577673729	19:31,039,384	A/G	—	uncertain significance
rs542930761	19:31,039,468	G/A	—	uncertain significance
rs142744560	19:31,039,490	G/A	—	benign
rs112677884	19:31,039,506	G/A	—	likely benign
rs752209246	19:31,039,530	G/A	—	uncertain significance
rs769419345	19:31,039,614	C/T	—	uncertain significance
rs149816388	19:31,039,631	C/T	—	likely benign
rs377642821	19:31,039,663	G/A	—	uncertain significance
rs77238711	19:31,039,669	C/T	—	benign
rs770903154	19:31,039,712	C/T	—	likely benign
rs147863190	19:31,039,805	C/T	—	likely benign
rs140355821	19:31,039,813	G/C	—	uncertain significance
rs1361170706	19:31,039,822	A/C	—	uncertain significance
rs781377488	19:31,039,894	G/A	—	uncertain significance
rs1277053396	19:31,039,918	C/G	—	uncertain significance
rs772436450	19:31,039,926	G/A	—	uncertain significance
rs776353797	19:31,039,960	T/A	—	uncertain significance
rs201256892	19:31,039,984	C/T	—	uncertain significance
rs775487730	19:31,040,060	C/T	—	likely benign
rs753985257	19:31,040,136	G/T	—	uncertain significance
rs142812385	19:31,040,194	C/T	—	uncertain significance
rs371124100	19:31,040,212	C/T	—	uncertain significance
rs2146249851	19:31,040,219	G/T	—	uncertain significance
rs146045772	19:31,040,226	C/G	—	likely benign
rs750922836	19:31,040,283	C/T	—	uncertain significance
rs767947085	19:31,040,324	G/T	—	likely benign
rs374416051	19:31,040,367	G/A	—	uncertain significance
rs11671893	19:31,041,053	T/C	intron variant	—
rs55663539	19:31,041,654	T/C	intron variant	—

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

Gene information from NCBI Gene. Variant classifications from ClinVar.