List of variants in gene LRAT 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_004744.5(LRAT):c.233_242del (p.Leu78fs)	rs786205644
NM_004744.5(LRAT):c.459dup (p.Tyr154fs)	rs765063151
NM_004744.5(LRAT):c.608T>A (p.Leu203Ter)	rs2111038250

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