List of variants in gene MYO7A studied 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
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.6640G>A (p.Gly2214Ser)	rs111033231	0.01911
NM_000260.4(MYO7A):c.1007G>A (p.Arg336His)	rs45629132	0.00164
NM_000260.4(MYO7A):c.2057G>A (p.Arg686His)	rs781991817	0.00036
NM_000260.4(MYO7A):c.6247G>A (p.Ala2083Thr)	rs41298759	0.00021
NM_000260.4(MYO7A):c.2507G>A (p.Arg836His)	rs782179888	0.00004
NM_000260.4(MYO7A):c.3G>A (p.Met1Ile)	rs782787126	0.00002
NM_000260.4(MYO7A):c.6626G>A (p.Arg2209Gln)	rs776881443	0.00002
NM_000260.4(MYO7A):c.2617C>T (p.Arg873Trp)	rs200454015
NM_000260.4(MYO7A):c.4635G>A (p.Trp1545Ter)	rs918353878

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