PRRC2B

proline rich coiled-coil 2B

Summary

Enables RNA binding activity. Predicted to be involved in cell differentiation. Predicted to act upstream of or within in utero embryonic development. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants173 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs182293592	9:134,269,789	G/T	regulatory region variant	—
rs2538842578	9:134,308,019	G/A	—	uncertain significance
rs775415625	9:134,308,063	C/T	—	uncertain significance
rs1838217531	9:134,308,064	C/T	—	uncertain significance
rs2538842800	9:134,308,103	G/C	—	uncertain significance
rs748496050	9:134,308,117	A/G	—	uncertain significance
rs41302675	9:134,308,126	G/A	—	likely benign
rs762708071	9:134,312,012	G/C	—	uncertain significance
rs376010304	9:134,312,045	C/T	—	uncertain significance
rs200715842	9:134,312,087	C/T	—	uncertain significance
rs180921892	9:134,319,598	T/G	—	uncertain significance
rs1199044980	9:134,319,670	G/A	—	uncertain significance
rs545470217	9:134,321,823	A/C	—	uncertain significance
rs2538872260	9:134,321,866	G/A	—	uncertain significance
rs368227837	9:134,321,884	C/T	—	uncertain significance
rs536522617	9:134,321,919	G/A	—	conflicting classifications of pathogenicity
rs369974538	9:134,321,944	C/T	—	uncertain significance
rs199807582	9:134,322,503	G/A	—	uncertain significance
rs1006237960	9:134,322,520	T/C	—	uncertain significance
rs780309024	9:134,322,541	C/T	—	uncertain significance
rs762251528	9:134,323,057	A/G	—	uncertain significance
rs557756101	9:134,323,074	C/T	—	uncertain significance
rs765458862	9:134,323,083	C/T	—	uncertain significance
rs1194882575	9:134,323,113	C/T	—	uncertain significance
rs368879490	9:134,323,132	A/C	—	uncertain significance
rs574287239	9:134,323,134	G/T	—	uncertain significance
rs1000635927	9:134,323,147	A/C	—	uncertain significance
rs1273271703	9:134,323,170	G/A	—	uncertain significance
rs7853919	9:134,325,605	G/C	intron variant	—
rs774688865	9:134,330,469	A/G	—	uncertain significance
rs371609357	9:134,334,576	C/T	—	uncertain significance
rs377034305	9:134,334,603	A/G	—	uncertain significance
rs775259843	9:134,334,607	C/T	—	likely benign
rs372489984	9:134,334,612	G/A	—	uncertain significance
rs767173493	9:134,334,618	C/T	—	uncertain significance
rs370435017	9:134,334,654	G/T	—	uncertain significance
rs778138922	9:134,334,661	C/T	—	likely benign
rs143804019	9:134,340,173	C/A	—	uncertain significance
rs772000942	9:134,340,174	C/T	—	uncertain significance
rs561244073	9:134,340,192	G/A	—	uncertain significance
rs756930239	9:134,340,200	G/C	—	uncertain significance
rs528897720	9:134,340,251	G/A	—	likely benign
rs2538909706	9:134,340,313	C/T	—	uncertain significance
rs748992952	9:134,340,382	G/A	—	likely benign
rs10793870	9:134,342,938	T/C	—	benign
rs200396561	9:134,343,002	A/T	—	likely benign
rs2538914968	9:134,343,034	A/G	—	likely benign
rs1943435249	9:134,343,048	G/A	—	uncertain significance
rs746430327	9:134,343,072	G/T	—	uncertain significance
rs2538915164	9:134,343,096	T/A	—	uncertain significance
rs371967847	9:134,346,328	C/T	—	uncertain significance
rs780986439	9:134,348,931	A/G	—	likely benign
rs774966868	9:134,348,946	G/A	—	uncertain significance
rs796517352	9:134,348,972	C/T	—	uncertain significance
rs376856745	9:134,348,991	T/C	—	uncertain significance
rs1943603200	9:134,348,999	A/C	—	uncertain significance
rs755859078	9:134,349,014	G/T	—	uncertain significance
rs772074786	9:134,349,050	A/C	—	uncertain significance
rs760839619	9:134,349,059	C/T	—	likely benign
rs771120179	9:134,349,060	C/T	—	conflicting classifications of pathogenicity
rs372626601	9:134,349,066	C/T	—	uncertain significance
rs371470825	9:134,349,078	C/T	—	uncertain significance
rs781431550	9:134,349,920	G/A	—	uncertain significance
rs1331151565	9:134,350,038	G/T	—	uncertain significance
rs2538927532	9:134,350,080	T/C	—	uncertain significance
rs2538927542	9:134,350,085	C/T	—	uncertain significance
rs148672611	9:134,350,117	G/A	—	benign
rs373198606	9:134,350,178	C/T	—	uncertain significance
rs376674089	9:134,350,179	G/A	—	uncertain significance
rs773476090	9:134,350,190	C/T	—	uncertain significance
rs17458486	9:134,350,231	C/T	—	benign
rs368821312	9:134,350,314	C/T	—	uncertain significance
rs10736851	9:134,350,323	G/C	—	benign
rs1463630483	9:134,350,326	G/A	—	uncertain significance
rs1352691084	9:134,350,390	G/C	—	uncertain significance
rs2538928442	9:134,350,415	G/T	—	uncertain significance
rs578168304	9:134,350,427	A/C	—	uncertain significance
rs10751478	9:134,350,458	C/T	—	benign
rs1284390430	9:134,350,472	G/A	—	uncertain significance
rs763650568	9:134,350,475	G/A	—	uncertain significance
rs1374756662	9:134,350,503	C/T	—	uncertain significance
rs748227471	9:134,350,509	C/T	—	uncertain significance
rs760957486	9:134,350,515	C/T	—	uncertain significance
rs267602148	9:134,350,538	C/T	—	likely benign
rs1471010638	9:134,350,559	C/T	—	uncertain significance
rs760146261	9:134,350,648	G/A	—	uncertain significance
rs200476893	9:134,350,684	A/T	—	uncertain significance
rs201513306	9:134,350,709	C/T	—	uncertain significance
rs553258692	9:134,350,710	G/A	—	uncertain significance
rs765537018	9:134,350,751	C/T	—	uncertain significance
rs200121607	9:134,350,758	C/T	—	uncertain significance
rs941870780	9:134,350,836	G/A	—	uncertain significance
rs373454097	9:134,350,838	C/T	—	benign
rs767581375	9:134,350,844	C/T	—	uncertain significance
rs541104893	9:134,350,863	C/T	—	uncertain significance
rs769349458	9:134,350,866	G/T	—	uncertain significance
rs1943665336	9:134,350,878	G/T	—	likely benign
rs761299154	9:134,350,959	G/A	—	uncertain significance
rs1361832699	9:134,351,045	T/C	—	uncertain significance
rs1469607536	9:134,351,051	C/T	—	uncertain significance

Showing 100 of 173 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.