PRR30

proline rich 30

Known Variants32 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2465892350	2:27,360,056	G/T	—	uncertain significance
rs777036721	2:27,360,065	G/A	—	likely benign
rs969681333	2:27,360,128	G/A	—	uncertain significance
rs928887113	2:27,360,140	G/T	—	uncertain significance
rs562271681	2:27,360,156	C/T	—	uncertain significance
rs138389066	2:27,360,162	G/A	—	uncertain significance
rs2465892540	2:27,360,180	G/A	—	uncertain significance
rs375208373	2:27,360,207	A/C	—	uncertain significance
rs369892953	2:27,360,216	T/G	—	likely benign
rs768172063	2:27,360,297	G/A	—	uncertain significance
rs749600179	2:27,360,309	C/T	—	uncertain significance
rs745398301	2:27,360,320	C/T	—	uncertain significance
rs2465892855	2:27,360,399	T/C	—	uncertain significance
rs2465892863	2:27,360,405	G/T	—	likely benign
rs145326504	2:27,360,429	G/A	—	uncertain significance
rs751095543	2:27,360,491	A/G	—	uncertain significance
rs762450544	2:27,360,566	A/G	—	uncertain significance
rs752078499	2:27,360,603	C/T	—	uncertain significance
rs372566599	2:27,360,627	C/T	—	uncertain significance
rs1280021877	2:27,360,743	A/G	—	uncertain significance
rs61741796	2:27,360,773	G/A	missense variant	—
rs1415278063	2:27,360,809	G/A	—	uncertain significance
rs762858640	2:27,360,840	G/A	—	uncertain significance
rs768675313	2:27,360,879	G/T	—	uncertain significance
rs911744446	2:27,360,885	G/T	—	uncertain significance
rs1445673440	2:27,361,023	G/A	—	uncertain significance
rs553610498	2:27,361,026	G/A	—	uncertain significance
rs149337790	2:27,361,028	C/T	—	likely benign
rs570671962	2:27,361,029	G/A	—	uncertain significance
rs2465894129	2:27,361,043	G/A	—	likely benign
rs149656537	2:27,361,080	G/A	—	uncertain significance
rs781734497	2:27,361,143	G/A	—	likely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.