ClinVar Miner

List of variants in gene TYR reported as likely benign for Inborn genetic diseases

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_000372.5(TYR):c.1214G>A (p.Arg405His)	rs772173320	0.00007
NM_000372.5(TYR):c.127A>G (p.Arg43Gly)	rs2496527977

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