Variants in gene RARS2 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_020320.5(RARS2):c.872A>G (p.Lys291Arg)	rs17850652	0.09110
NM_020320.5(RARS2):c.991A>G (p.Ile331Val)	rs3757370	0.02330
NM_020320.5(RARS2):c.63A>G (p.Pro21=)	rs7748563	0.01309
NM_020320.5(RARS2):c.606C>T (p.Leu202=)	rs75794097	0.01095
NM_020320.5(RARS2):c.-8A>C	rs28381459	0.00245
NM_020320.5(RARS2):c.1410C>A (p.Leu470=)	rs139564081	0.00223
NM_020320.5(RARS2):c.155A>T (p.Lys52Ile)	rs73496064	0.00172
NM_020320.5(RARS2):c.456T>C (p.Asn152=)	rs141374913	0.00070
NM_020320.5(RARS2):c.975-14C>T	rs199941996	0.00045
NM_020320.5(RARS2):c.207A>G (p.Ala69=)	rs568483789	0.00025
NM_020320.5(RARS2):c.396-13A>T	rs181740811	0.00019
NM_020320.5(RARS2):c.452-22TA[2]	rs772255685
NM_020320.5(RARS2):c.726A>G (p.Gln242=)	rs145499324
NM_020320.5(RARS2):c.888G>C (p.Thr296=)	rs145189950

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