List of variants in gene GARS1 reported as likely benign 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_002047.4(GARS1):c.1031+14T>G	rs189589556	0.00213
NM_002047.4(GARS1):c.1420C>A (p.Arg474=)	rs113958280	0.00210
NM_002047.4(GARS1):c.1962C>T (p.Ile654=)	rs201927627	0.00120
NM_002047.4(GARS1):c.699C>T (p.Val233=)	rs187937286	0.00063
NM_002047.4(GARS1):c.253A>G (p.Lys85Glu)	rs200294578	0.00029
NM_002047.4(GARS1):c.1100A>G (p.Asn367Ser)	rs192443850	0.00024
NM_002047.4(GARS1):c.302G>A (p.Arg101His)	rs200887429	0.00022
NM_002047.4(GARS1):c.236G>A (p.Arg79Gln)	rs369466037	0.00011
NM_002047.4(GARS1):c.765G>A (p.Ala255=)	rs201447520	0.00010
NM_002047.4(GARS1):c.270C>T (p.Asp90=)	rs369898799	0.00009
NM_002047.4(GARS1):c.1478A>G (p.Asn493Ser)	rs538571144	0.00006
NM_002047.4(GARS1):c.764C>T (p.Ala255Val)	rs765478968	0.00006
NM_002047.4(GARS1):c.787G>A (p.Val263Ile)	rs77518956	0.00004
NM_002047.4(GARS1):c.174G>A (p.Ala58=)	rs747227947	0.00003
NM_002047.4(GARS1):c.1817G>A (p.Ser606Asn)	rs773316961	0.00002
NM_002047.4(GARS1):c.138G>A (p.Leu46=)

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