ClinVar Miner

List of variants in gene MYH9 reported as uncertain significance for Meniere disease

Included ClinVar conditions (1):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp)	rs76368635	0.00123
NM_002473.6(MYH9):c.4225G>A (p.Asp1409Asn)	rs34292387	0.00025

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