ClinVar Miner

List of variants in gene EPHA2 studied for vestibular disorder

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
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004431.5(EPHA2):c.2162G>A (p.Arg721Gln)	rs116506614	0.00073
NM_004431.5(EPHA2):c.556G>A (p.Gly186Ser)
NM_004431.5(EPHA2):c.943C>T (p.Arg315Trp)

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