List of variants in gene FOLR1 reported by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_016729.3(FOLR1):c.292C>T (p.Arg98Trp)	rs76191655	0.00274
NM_016729.3(FOLR1):c.508G>A (p.Ala170Thr)	rs139633601	0.00172
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.157T>C (p.Leu53=)	rs143413500	0.00029
NM_016729.3(FOLR1):c.357+8T>A	rs886042924	0.00016
NM_016729.3(FOLR1):c.719C>T (p.Ala240Val)	rs147155003	0.00010
NM_016729.3(FOLR1):c.215A>G (p.Gln72Arg)	rs148345688	0.00006
NM_016729.3(FOLR1):c.13A>G (p.Met5Val)	rs371565364	0.00004
NM_016729.3(FOLR1):c.507C>T (p.Cys169=)	rs398124307	0.00004
NM_016729.3(FOLR1):c.261C>T (p.Asn87=)	rs375444839	0.00001
NM_016729.3(FOLR1):c.352C>T (p.Gln118Ter)	rs121918405	0.00001
NM_016729.3(FOLR1):c.314G>T (p.Cys105Phe)	rs755627957
NM_016729.3(FOLR1):c.34del (p.Leu12fs)	rs1555068629
NM_016729.3(FOLR1):c.510A>G (p.Ala170=)	rs564331848

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