ClinVar Miner

List of variants in gene combination MMP26, OR51F1 reported as likely benign

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_001004752.2(OR51F1):c.815G>A (p.Arg272His)	rs201118576	0.00007
NM_001004752.2(OR51F1):c.926G>A (p.Arg309His)	rs369896596

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