List of variants in gene LRBA reported as uncertain significance for Meniere disease

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001364905.1(LRBA):c.109C>T (p.Pro37Ser)	rs374519451	0.00004
NM_001364905.1(LRBA):c.319C>A (p.Gln107Lys)	rs373476644	0.00004
NM_001364905.1(LRBA):c.1348C>T (p.Leu450Phe)
NM_001364905.1(LRBA):c.4048A>T (p.Asn1350Tyr)

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