ClinVar Miner

List of variants in gene S100A2 studied 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
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_005978.4(S100A2):c.26C>T (p.Ala9Val)	rs575985349

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