List of variants in gene TMIE reported as likely benign for auditory system 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_147196.3(TMIE):c.*695G>A	rs77244938	0.05181
NM_147196.3(TMIE):c.*51C>T	rs56002857	0.04613
NM_147196.3(TMIE):c.-37C>A	rs530579940	0.01988

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