List of variants in gene combination MATN3, WDR35-DT reported as pathogenic for bone disorder

Minimum submission review status:		Collection method:
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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.908C>T (p.Thr303Met)	rs77245812	0.01128
NC_000002.12:g.19998776_20009244dup
NM_002381.5(MATN3):c.910T>A (p.Cys304Ser)	rs104893639

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