ClinVar Miner

List of variants in gene TMIE reported as likely pathogenic for Hearing loss, autosomal recessive

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_147196.3(TMIE):c.241C>T (p.Arg81Cys)	rs28942096	0.00001
NM_147196.3(TMIE):c.250C>T (p.Arg84Trp)	rs28942097	0.00001

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