Variants in gene MARS1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004990.4(MARS1):c.2671C>T (p.Pro891Ser)	rs35843015	0.00070
NM_004990.4(MARS1):c.661G>A (p.Glu221Lys)	rs200334446	0.00016
NM_004990.4(MARS1):c.1177G>A (p.Ala393Thr)	rs141340466	0.00011
NM_004990.4(MARS1):c.734A>G (p.Glu245Gly)	rs778753999	0.00007
NM_004990.4(MARS1):c.1540-3C>T	rs372013808	0.00006
NM_004990.4(MARS1):c.747G>A (p.Pro249=)	rs200490364	0.00004
NM_004990.4(MARS1):c.1445C>T (p.Thr482Ile)	rs1173899198	0.00001
NM_004990.4(MARS1):c.212del (p.Leu71fs)	rs751080704

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