ClinVar Miner

List of variants in gene MMP13 reported as likely benign for metaphyseal chondrodysplasia, Spahr type

Included ClinVar conditions (2):

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_002427.4(MMP13):c.1080T>C (p.Tyr360=)	rs61737008	0.00951
NM_002427.4(MMP13):c.1372C>T (p.Arg458Cys)	rs142064825	0.00071

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