List of variants in gene RFT1 reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_052859.4(RFT1):c.1331C>T (p.Thr444Met)	rs147740901	0.00040
NM_052859.4(RFT1):c.1283G>A (p.Ser428Asn)	rs201230044	0.00019
NM_052859.4(RFT1):c.1214A>G (p.Asn405Ser)	rs111924005	0.00004
NM_052859.4(RFT1):c.1324C>T (p.Arg442Trp)	rs146610276	0.00004
NM_052859.4(RFT1):c.464C>G (p.Ala155Gly)	rs1441819935	0.00001
NM_052859.4(RFT1):c.710G>A (p.Trp237Ter)	rs1408405816
NM_052859.4(RFT1):c.74G>A (p.Arg25Gln)	rs780107020
NM_052859.4(RFT1):c.827-6T>G	rs753486430

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