List of variants in gene YARS1 reported as uncertain significance for Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003680.4(YARS1):c.946G>A (p.Ala316Thr)	rs138454151	0.00006
NM_003680.4(YARS1):c.181G>A (p.Asp61Asn)	rs776582429	0.00001
NM_003680.4(YARS1):c.1078C>G (p.Pro360Ala)
NM_003680.4(YARS1):c.1435GAG[1] (p.Glu480del)
NM_003680.4(YARS1):c.591+6T>A
NM_003680.4(YARS1):c.611A>C (p.Tyr204Ser)	rs1217293329
NM_003680.4(YARS1):c.640A>G (p.Met214Val)

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