Variants in gene MTRR with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 17

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HGVS	dbSNP	gnomAD frequency
NM_002454.3(MTRR):c.1982A>G (p.His661Arg)	rs148909799	0.00196
NM_002454.3(MTRR):c.869T>C (p.Ile290Thr)	rs144899305	0.00096
NM_002454.3(MTRR):c.446C>T (p.Ala149Val)	rs142714881	0.00077
NM_002454.3(MTRR):c.540G>A (p.Val180=)	rs149037732	0.00046
NM_002454.3(MTRR):c.906T>C (p.Asn302=)	rs144729918	0.00025
NM_002454.3(MTRR):c.1020C>T (p.Cys340=)	rs201348649	0.00010
NM_002454.3(MTRR):c.1677-2dup	rs747255318	0.00009
NM_002454.3(MTRR):c.21A>G (p.Leu7=)	rs114427781	0.00007
NM_002454.3(MTRR):c.346C>A (p.Gln116Lys)	rs202110383	0.00005
NM_002454.3(MTRR):c.27T>C (p.Ala9=)	rs114748706	0.00004
NM_002454.3(MTRR):c.1086G>A (p.Ala362=)	rs750381895	0.00001
NM_002454.3(MTRR):c.1769+8A>G	rs892239997	0.00001
NM_002454.3(MTRR):c.1890G>A (p.Gln630=)	rs9282786	0.00001
NM_002454.3(MTRR):c.399A>G (p.Val133=)	rs560392566	0.00001
NM_002454.3(MTRR):c.1875G>T (p.Val625=)	rs12347
NM_002454.3(MTRR):c.1998A>G (p.Gln666=)	rs767507060
NM_002454.3(MTRR):c.99A>C (p.Ala33=)	rs1747850617

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