List of variants in gene EARS2 reported by Neuberg Centre For Genomic Medicine, NCGM

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001083614.2(EARS2):c.328G>A (p.Gly110Ser)	rs201842633	0.00025
NM_001083614.2(EARS2):c.322C>T (p.Arg108Trp)	rs376103091	0.00019
NM_001083614.2(EARS2):c.1193A>G (p.Tyr398Cys)	rs571483034	0.00005
NM_001083614.2(EARS2):c.719del (p.Gly240fs)
NM_001083614.2(EARS2):c.739G>A (p.Gly247Ser)

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