List of variants in gene RARS2 reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_020320.5(RARS2):c.754T>A (p.Tyr252Asn)	rs140692271	0.00018
NM_020320.5(RARS2):c.1366C>T (p.Arg456Cys)	rs147844153	0.00011
NM_020320.5(RARS2):c.1492A>G (p.Ile498Val)	rs200632524	0.00006
NM_020320.5(RARS2):c.1257C>A (p.Asn419Lys)	rs751904499	0.00004
NM_020320.5(RARS2):c.1718C>T (p.Thr573Ile)	rs541516452	0.00004
NM_020320.5(RARS2):c.1405C>T (p.Arg469Cys)	rs767150990	0.00002
NM_020320.5(RARS2):c.1024A>G (p.Met342Val)	rs387907048	0.00001
NM_020320.5(RARS2):c.1650+5G>A	rs750433723	0.00001
NM_020320.5(RARS2):c.1724dup (p.Cys576fs)	rs863224184	0.00001
NM_020320.5(RARS2):c.1037C>T (p.Thr346Ile)	rs1773402352
NM_020320.5(RARS2):c.1305+20T>C	rs1057518531
NM_020320.5(RARS2):c.1438G>A (p.Gly480Arg)	rs769853119
NM_020320.5(RARS2):c.213+4C>T
NM_020320.5(RARS2):c.488A>G (p.His163Arg)	rs1260340118
NM_020320.5(RARS2):c.536-5G>A	rs1781141008
NM_020320.5(RARS2):c.734G>A (p.Arg245Gln)
NM_020320.5(RARS2):c.772-3del	rs368859792
NM_020320.5(RARS2):c.772-4_772-3del	rs368859792
NM_020320.5(RARS2):c.878+3A>G
NM_020320.5(RARS2):c.888G>C (p.Thr296=)	rs145189950

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