Variants in gene LARS2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_015340.4(LARS2):c.972C>A (p.His324Gln)	rs71645922	0.02237
NM_015340.4(LARS2):c.765G>A (p.Ala255=)	rs116272561	0.00466
NM_015340.4(LARS2):c.1552G>A (p.Asp518Asn)	rs116826217	0.00451
NM_015340.4(LARS2):c.2307C>T (p.Ser769=)	rs143838895	0.00280
NM_015340.4(LARS2):c.2602G>A (p.Glu868Lys)	rs34965084	0.00260
NM_015340.4(LARS2):c.1692C>T (p.Ala564=)	rs149911756	0.00203
NM_015340.4(LARS2):c.235-12G>A	rs75240042	0.00168
NM_015340.4(LARS2):c.255C>T (p.Tyr85=)	rs114881088	0.00157
NM_015340.4(LARS2):c.324C>T (p.Ser108=)	rs140105027	0.00064
NM_015340.4(LARS2):c.1622+8G>A	rs202009605	0.00030
NM_015340.4(LARS2):c.1779G>C (p.Leu593=)	rs148167639	0.00018
NM_015340.4(LARS2):c.1197A>G (p.Glu399=)	rs187209664	0.00002
NM_015340.4(LARS2):c.362A>G (p.Gln121Arg)	rs200681375	0.00002
NM_015340.4(LARS2):c.945G>A (p.Ser315=)	rs145135580
NM_015340.4(LARS2):c.945G>C (p.Ser315=)	rs145135580

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