List of variants in gene GARS1 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002047.4(GARS1):c.302G>A (p.Arg101His)	rs200887429	0.00022
NM_002047.4(GARS1):c.1478A>G (p.Asn493Ser)	rs538571144	0.00006
NM_002047.4(GARS1):c.1754T>C (p.Met585Thr)	rs374378925	0.00005
NM_002047.4(GARS1):c.52C>A (p.Leu18Met)	rs368574634	0.00003
NM_002047.4(GARS1):c.59T>C (p.Leu20Pro)	rs756664556	0.00003
NM_002047.4(GARS1):c.101G>A (p.Arg34Gln)	rs1189675611	0.00001
NM_002047.4(GARS1):c.1960A>G (p.Ile654Val)	rs1406586832	0.00001
NM_002047.4(GARS1):c.403G>T (p.Asp135Tyr)	rs778553007	0.00001
NM_002047.4(GARS1):c.1171C>A (p.Arg391Ser)	rs370057212
NM_002047.4(GARS1):c.1304A>G (p.Asn435Ser)	rs2534313888
NM_002047.4(GARS1):c.439C>G (p.Leu147Val)

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