Variants in gene MARS1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004990.4(MARS1):c.2180G>A (p.Arg727Gln)	rs113808165	0.00541
NM_004990.4(MARS1):c.1753+7A>G	rs117914586	0.00435
NM_004990.4(MARS1):c.626G>A (p.Ser209Asn)	rs141671963	0.00327
NM_004990.4(MARS1):c.2204+11G>A	rs202080192	0.00239
NM_004990.4(MARS1):c.280-14C>T	rs183195960	0.00223
NM_004990.4(MARS1):c.1812G>A (p.Gly604=)	rs117633211	0.00083
NM_004990.4(MARS1):c.477C>T (p.Pro159=)	rs117101415	0.00083
NM_004990.4(MARS1):c.1689C>T (p.Val563=)	rs117833843	0.00071
NM_004990.4(MARS1):c.901C>T (p.Arg301Cys)	rs139661803	0.00052
NM_004990.4(MARS1):c.873C>T (p.Ala291=)	rs79531790

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