ClinVar Miner

List of variants in gene S100A9 reported as likely benign for not specified

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.32A>G (p.Asn11Ser)	rs781496198	0.00006
NM_002965.4(S100A9):c.4A>T (p.Thr2Ser)	rs759389626	0.00002

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