List of variants in gene MATN3 reported as not provided for bone disorder

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_002381.5(MATN3):c.209G>A (p.Arg70His)	rs104893640	0.00012
NM_002381.5(MATN3):c.656C>A (p.Ala219Asp)	rs28939677	0.00003
NM_002381.5(MATN3):c.693G>C (p.Lys231Asn)	rs773642745	0.00003
NM_002381.5(MATN3):c.359C>T (p.Thr120Met)	rs397515546	0.00001
NM_002381.5(MATN3):c.659T>C (p.Val220Ala)	rs187943382	0.00001
NM_002381.5(MATN3):c.361C>T (p.Arg121Trp)	rs104893637
NM_002381.5(MATN3):c.400G>A (p.Glu134Lys)	rs2103484088
NM_002381.5(MATN3):c.437T>G (p.Leu146Arg)	rs2103484073
NM_002381.5(MATN3):c.513_530del (p.Asp171_Val176del)	rs2103484013
NM_002381.5(MATN3):c.518C>A (p.Ala173Asp)	rs779413744
NM_002381.5(MATN3):c.575T>A (p.Ile192Asn)	rs2103483989
NM_002381.5(MATN3):c.581T>A (p.Val194Asp)	rs104893645
NM_002381.5(MATN3):c.584C>A (p.Thr195Lys)	rs765225021
NM_002381.5(MATN3):c.626G>C (p.Arg209Pro)	rs749845872
NM_002381.5(MATN3):c.652T>A (p.Tyr218Asn)	rs2103483937

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