ClinVar Miner

List of variants in gene ACTB reported as likely benign by Genetic Services Laboratory, University of Chicago

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_001101.5(ACTB):c.942G>A (p.Gln314=)	rs11546939	0.03304
NM_001101.5(ACTB):c.1023C>T (p.Ile341=)	rs58704474	0.01128

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