List of variants in gene GARS1 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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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.1700-45T>C	rs118002895	0.02313
NM_002047.4(GARS1):c.11C>T (p.Pro4Leu)	rs62636572	0.01280
NM_002047.4(GARS1):c.803C>T (p.Thr268Ile)	rs2230310	0.00357
NM_002047.4(GARS1):c.1031+14T>G	rs189589556	0.00213
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.1100A>G (p.Asn367Ser)	rs192443850	0.00024
NM_002047.4(GARS1):c.408A>G (p.Gln136=)	rs200279483	0.00021
NM_002047.4(GARS1):c.1904-28T>G	rs375716806	0.00018
NM_002047.4(GARS1):c.816A>G (p.Leu272=)	rs777128525	0.00005
NM_002047.4(GARS1):c.1737C>T (p.Phe579=)	rs752464405	0.00004
NM_002047.4(GARS1):c.1581T>C (p.Ile527=)	rs960876782	0.00002
NM_002047.4(GARS1):c.1614-4G>A	rs376324026
NM_002047.4(GARS1):c.2217A>G (p.Glu739=)
NM_002047.4(GARS1):c.47TGC[4] (p.Leu20del)	rs150213018
NM_002047.4(GARS1):c.969T>G (p.Ala323=)

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