List of variants in gene EPS8L2 reported as uncertain significance for vestibular disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_022772.4(EPS8L2):c.13G>A (p.Gly5Arg)	rs375020679	0.00012
NM_022772.4(EPS8L2):c.1141C>T (p.Arg381Cys)
NM_022772.4(EPS8L2):c.805T>C (p.Phe269Leu)
NM_022772.4(EPS8L2):c.814C>T (p.Arg272Trp)	rs766514830
NM_022772.4(EPS8L2):c.922C>T (p.Pro308Ser)

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