ClinVar Miner

List of variants in gene S100A9 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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_002965.4(S100A9):c.151-5C>T	rs140163350	0.00430
NM_002965.4(S100A9):c.295G>A (p.Glu99Lys)	rs143906646	0.00053

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