List of variants in gene CARS2 reported as likely pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_024537.4(CARS2):c.1084C>T (p.Gln362Ter)	rs1439475292	0.00001
NM_024537.4(CARS2):c.655G>A (p.Ala219Thr)	rs727505361	0.00001
NM_024537.4(CARS2):c.878_879del (p.Phe293fs)	rs1258446331

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