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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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.66A>G (p.Ile22Met)	rs1801394	0.44938
NM_002454.3(MTRR):c.524C>T (p.Ser175Leu)	rs1532268	0.31601
NM_002454.3(MTRR):c.1049A>G (p.Lys350Arg)	rs162036	0.20973
NM_002454.3(MTRR):c.1783C>T (p.His595Tyr)	rs10380	0.18188
NM_002454.3(MTRR):c.*151A>G	rs112465197	0.01706
NM_002454.3(MTRR):c.*49A>G	rs142538539	0.01601
NM_002454.3(MTRR):c.*167A>G	rs115253331	0.01048
NM_002454.3(MTRR):c.288C>T (p.Leu96=)	rs35587995	0.00500
NM_002454.3(MTRR):c.1468A>G (p.Thr490Ala)	rs41283145	0.00414
NM_002454.3(MTRR):c.1819G>A (p.Val607Ile)	rs114259126	0.00366
NM_002454.3(MTRR):c.876C>T (p.Thr292=)	rs144724549	0.00312
NM_002454.3(MTRR):c.210C>G (p.Arg70=)	rs41282641	0.00297
NM_002454.3(MTRR):c.1326C>T (p.Leu442=)	rs144781389	0.00274
NM_002454.3(MTRR):c.739C>T (p.Pro247Ser)	rs114053717	0.00190
NM_002454.3(MTRR):c.177C>G (p.Thr59=)	rs142098262	0.00135
NM_002454.3(MTRR):c.144C>T (p.Thr48=)	rs138612190	0.00111
NM_002454.3(MTRR):c.1091_1093del (p.Cys364del)	rs796052001

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