List of variants in gene MATN3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002381.5(MATN3):c.330C>T (p.Ile110=)	rs201755444	0.00039
NM_002381.5(MATN3):c.663C>T (p.Gly221=)	rs369658011	0.00018
NM_002381.5(MATN3):c.651C>T (p.Leu217=)

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