ClinVar Miner

List of variants in gene LARS1 reported as likely benign for liver failure

Included ClinVar conditions (11):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_020117.11(LARS1):c.2212+13T>C	rs114726414	0.00678
NM_020117.11(LARS1):c.3286A>G (p.Ile1096Val)	rs373129039	0.00001

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