ClinVar Miner

List of variants in gene AGXT reported as likely benign by Counsyl

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000030.3(AGXT):c.777-17C>A	rs112319664	0.00036
NM_000030.3(AGXT):c.942+14T>G	rs886055843	0.00002

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