RNF13

ring finger protein 13

Summary

The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. The specific function of this gene has not yet been determined. Alternatively spliced transcript variants that encode the same protein have been reported. A pseudogene, which is also located on chromosome 3, has been defined for this gene. [provided by RefSeq, Jul 2008]

Known Variants196 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs10935779	3:149,543,102	C/G	—	—
rs2473178005	3:149,563,828	A/G	—	likely benign
rs1722610564	3:149,563,829	G/A	—	uncertain significance
rs1450138635	3:149,563,838	A/G	—	uncertain significance
rs2108375461	3:149,563,847	G/A	—	uncertain significance
rs745692701	3:149,563,854	A/G	—	uncertain significance
rs140665765	3:149,563,856	G/A	—	conflicting classifications of pathogenicity
rs2473178274	3:149,563,857	T/A	—	uncertain significance
rs2473178288	3:149,563,859	T/C	—	uncertain significance
rs2473178321	3:149,563,863	C/T	—	uncertain significance
rs760934570	3:149,563,865	A/G	—	benign
rs768978970	3:149,563,870	G/T	—	uncertain significance
rs763378011	3:149,563,898	C/A	—	uncertain significance
rs145759442	3:149,563,902	T/A	—	conflicting classifications of pathogenicity
rs1559903080	3:149,563,903	G/A	—	likely benign
rs755810102	3:149,563,912	A/G	—	likely benign
rs2473178773	3:149,563,919	A/G	—	uncertain significance
rs2473178831	3:149,563,932	G/T	—	uncertain significance
rs967807911	3:149,563,936	A/G	—	likely benign
rs2108375702	3:149,563,945	T/C	—	likely benign
rs2473204630	3:149,570,333	G/A	—	uncertain significance
rs1157616435	3:149,589,801	C/T	—	likely benign
rs757914682	3:149,589,819	T/G	—	uncertain significance
rs766434167	3:149,589,836	A/G	—	likely benign
rs2108442079	3:149,589,838	C/A	—	uncertain significance
rs781084617	3:149,589,858	A/G	—	uncertain significance
rs948687931	3:149,589,873	G/A	—	uncertain significance
rs2473299021	3:149,589,882	A/T	—	uncertain significance
rs2108442188	3:149,589,887	A/G	—	likely benign
rs2473299102	3:149,589,893	C/T	—	likely benign
rs199679843	3:149,589,894	A/T	—	uncertain significance
rs142620410	3:149,589,902	C/T	—	likely benign
rs146907927	3:149,589,903	G/T	—	uncertain significance
rs772549838	3:149,589,912	A/G	—	uncertain significance
rs775761047	3:149,589,918	C/T	—	conflicting classifications of pathogenicity
rs2108442274	3:149,589,926	T/C	—	likely benign
rs1248927481	3:149,589,941	G/C	—	uncertain significance
rs552262347	3:149,589,942	G/C	—	uncertain significance
rs764855830	3:149,589,949	T/A	—	likely benign
rs41411047	3:149,592,911	G/A	intron variant	—
rs532528082	3:149,600,070	G/A	—	—
rs2473400362	3:149,613,254	T/G	—	likely benign
rs755921447	3:149,613,256	G/C	—	likely benign
rs754055420	3:149,613,257	C/A	—	benign
rs1400786437	3:149,613,271	A/G	—	likely benign
rs779018351	3:149,613,278	G/T	—	benign
rs2473400598	3:149,613,281	G/A	—	uncertain significance
rs899554140	3:149,613,292	A/T	—	likely benign
rs138875909	3:149,613,301	T/A	—	likely benign
rs780598817	3:149,613,306	A/G	—	benign
rs2473400822	3:149,613,308	G/A	—	uncertain significance
rs747349456	3:149,613,311	G/A	—	uncertain significance
rs1458533397	3:149,613,315	C/A	—	uncertain significance
rs199955067	3:149,613,316	T/C	—	likely benign
rs369737612	3:149,613,325	C/A	—	likely benign
rs772769215	3:149,613,331	C/T	—	likely benign
rs371448644	3:149,613,343	C/T	—	likely benign
rs770685913	3:149,613,344	G/A	—	uncertain significance
rs1469161562	3:149,613,355	C/T	—	likely benign
rs774043594	3:149,613,364	C/T	—	likely benign
rs2108491465	3:149,613,370	T/C	—	uncertain significance
rs1715898050	3:149,619,841	C/G	—	likely benign
rs377225073	3:149,619,852	T/A	—	likely benign
rs370291601	3:149,619,853	A/G	—	likely benign
rs1357510471	3:149,619,855	A/G	—	likely benign
rs528453221	3:149,619,876	A/G	—	benign
rs2473426711	3:149,619,881	C/T	—	likely benign
rs774129363	3:149,619,887	A/G	—	likely benign
rs191904836	3:149,619,900	G/C	—	benign
rs954781045	3:149,619,902	T/G	—	likely benign
rs924593862	3:149,619,920	T/C	—	likely benign
rs144710366	3:149,619,928	A/G	—	conflicting classifications of pathogenicity
rs1156676347	3:149,619,936	A/G	—	uncertain significance
rs2473427138	3:149,619,938	A/G	—	likely benign
rs148516101	3:149,619,941	T/C	—	likely benign
rs1180084188	3:149,619,956	A/C	—	likely benign
rs1219611161	3:149,629,748	T/G	—	uncertain significance
rs1717039887	3:149,629,767	G/T	—	uncertain significance
rs908478602	3:149,629,774	T/C	—	likely benign
rs756485383	3:149,629,775	A/T	—	uncertain significance
rs2108518514	3:149,629,780	A/G	—	likely benign
rs150196894	3:149,629,781	G/A	—	benign
rs1344976743	3:149,629,784	C/G	—	benign
rs771604937	3:149,629,792	T/C	—	likely benign
rs746501113	3:149,629,805	G/C	—	uncertain significance
rs1250628602	3:149,629,812	A/G	—	conflicting classifications of pathogenicity
rs768700103	3:149,629,816	A/G	—	likely benign
rs146054064	3:149,629,820	C/T	—	uncertain significance
rs761601970	3:149,629,824	T/C	—	uncertain significance
rs2108518590	3:149,629,836	T/A	—	uncertain significance
rs751728141	3:149,629,865	T/C	—	conflicting classifications of pathogenicity
rs1717053462	3:149,629,869	T/C	—	uncertain significance
rs969771734	3:149,629,877	A/C	—	likely benign
rs375591711	3:149,629,878	C/T	—	benign
rs73157016	3:149,629,884	C/T	—	benign
rs1485283499	3:149,638,908	C/G	—	likely benign
rs140042189	3:149,638,922	T/C	—	likely benign
rs771241791	3:149,638,927	A/G	—	uncertain significance
rs2473493483	3:149,638,936	C/T	—	uncertain significance
rs2473493628	3:149,638,955	G/A	—	uncertain significance

Showing 100 of 196 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.