FBXO47

F-box protein 47

Known Variants26 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs755406037	17:37,093,538	G/A	—	uncertain significance
rs1254021375	17:37,094,840	T/C	—	uncertain significance
rs776234579	17:37,094,861	C/T	—	uncertain significance
rs758904291	17:37,094,864	G/A	—	uncertain significance
rs770298267	17:37,094,872	A/C	—	uncertain significance
rs187260473	17:37,094,917	A/T	—	likely benign
rs145585502	17:37,094,938	C/G	—	uncertain significance
rs1204865066	17:37,099,068	G/A	—	uncertain significance
rs148926547	17:37,099,981	C/A	—	likely benign
rs35152618	17:37,100,894	G/C	—	—
rs759315789	17:37,101,226	T/C	—	uncertain significance
rs138301038	17:37,101,349	A/G	—	likely benign
rs9906595	17:37,101,380	T/C	missense variant	benign
rs2338373	17:37,104,834	G/C	intron variant	—
rs543238078	17:37,107,866	C/T	—	uncertain significance
rs772814791	17:37,107,924	C/T	—	uncertain significance
rs770220457	17:37,111,167	T/C	—	likely benign
rs1905486762	17:37,111,416	A/G	—	—
rs1023222255	17:37,118,156	G/C	—	uncertain significance
rs748501202	17:37,118,162	T/C	—	uncertain significance
rs2509166962	17:37,119,101	A/C	—	uncertain significance
rs2509167020	17:37,119,108	T/G	—	uncertain significance
rs746047037	17:37,119,167	T/C	—	uncertain significance
rs766059758	17:37,119,206	T/C	—	uncertain significance
rs140430888	17:37,119,246	C/T	—	benign
rs149385639	17:37,119,289	G/C	5 prime UTR variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.