List of variants in gene QARS1 reported as benign 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_005051.3(QARS1):c.977-13C>A	rs4521268	0.65945
NM_005051.3(QARS1):c.399C>T (p.His133=)	rs5030795	0.07620
NM_005051.3(QARS1):c.854A>G (p.Asn285Ser)	rs11539148	0.04122
NM_005051.3(QARS1):c.1957-19C>G	rs112579679	0.00826
NM_005051.3(QARS1):c.1635A>G (p.Gln545=)	rs113144521	0.00701
NM_005051.3(QARS1):c.1615-17C>G	rs138271247	0.00663
NM_005051.3(QARS1):c.1014T>C (p.Tyr338=)	rs138685078	0.00318
NM_005051.3(QARS1):c.1295+13T>C	rs149070379	0.00299
NM_005051.3(QARS1):c.163C>T (p.Leu55=)	rs58012546	0.00181

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