List of variants in gene FOLR1 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.72196438T>C	rs68068983	0.10633
NM_016729.3(FOLR1):c.169-186C>G	rs35805771	0.10537
NC_000011.10:g.72196454C>T	rs34030891	0.06606
NM_016729.3(FOLR1):c.169-71T>C	rs17162056	0.04211
NM_000802.3(FOLR1):c.-9+870A>C	rs7125189	0.04036
NM_000802.3(FOLR1):c.-9+695C>T	rs7109250	0.03781
NM_000802.3(FOLR1):c.-9+516G>A	rs1540087	0.03757
NM_000802.3(FOLR1):c.-9+153G>A	rs117787264	0.03562
NM_000802.3(FOLR1):c.-9+603C>T	rs9282688	0.02591
NM_016729.3(FOLR1):c.168+46G>C	rs77405781	0.01933
NM_016729.3(FOLR1):c.292C>T (p.Arg98Trp)	rs76191655	0.00274
NM_016729.3(FOLR1):c.493+2T>C	rs144637717	0.00134
NM_016729.3(FOLR1):c.321C>T (p.Tyr107=)	rs145674759	0.00052
NM_016729.3(FOLR1):c.396G>A (p.Val132=)	rs35179028	0.00033
NM_016729.3(FOLR1):c.157T>C (p.Leu53=)	rs143413500	0.00029
NM_000802.3(FOLR1):c.-20G>A	rs2071010
NM_016729.3(FOLR1):c.489T>C (p.Thr163=)	rs796052440

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