List of variants in gene RARS2 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020320.5(RARS2):c.442A>G (p.Thr148Ala)	rs143389605	0.00055
NM_020320.5(RARS2):c.773G>A (p.Arg258His)	rs145297855	0.00044
NM_020320.5(RARS2):c.1544A>G (p.Asp515Gly)	rs765088174	0.00005

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