List of variants in gene LRAT reported as benign for perceptual disorders

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004744.5(LRAT):c.*2670G>T	rs17032000	0.13064
NM_004744.5(LRAT):c.*817A>G	rs78274322	0.09886
NM_004744.5(LRAT):c.*1867C>T	rs78441257	0.09872
NM_004744.5(LRAT):c.*1338T>G	rs12507608	0.09793
NM_004744.5(LRAT):c.342G>A (p.Glu114=)	rs17031981	0.09214
NM_004744.5(LRAT):c.*3618G>A	rs17032002	0.02639
NM_004744.5(LRAT):c.74T>A (p.Phe25Tyr)	rs75368761	0.00748

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