List of variants in gene GARS1 reported as uncertain significance by Genesis Genome Database

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002047.4(GARS1):c.1754T>C (p.Met585Thr)	rs374378925	0.00004
NM_002047.4(GARS1):c.44C>T (p.Ala15Val)	rs758037738	0.00004
NM_002047.4(GARS1):c.1905G>A (p.Ser635=)	rs773889809	0.00001
NM_002047.4(GARS1):c.2044C>A (p.His682Asn)	rs1437642803	0.00001
NM_002047.4(GARS1):c.1171C>T (p.Arg391Cys)	rs370057212
NM_002047.4(GARS1):c.130A>C (p.Ile44Leu)	rs1584017371
NM_002047.4(GARS1):c.1403A>C (p.Asp468Ala)	rs1584043561
NM_002047.4(GARS1):c.1528A>C (p.Lys510Gln)	rs1584044584
NM_002047.4(GARS1):c.1614-4G>C	rs376324026
NM_002047.4(GARS1):c.1809+10_1809+12del	rs747338292
NM_002047.4(GARS1):c.548T>C (p.Leu183Pro)	rs137852644
NM_002047.4(GARS1):c.647A>G (p.His216Arg)	rs768987322

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