List of variants in gene C2CD3 reported as benign for dysostosis

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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_001286577.2(C2CD3):c.4923A>G (p.Val1641=)	rs4453265	0.46577
NM_001286577.2(C2CD3):c.704C>T (p.Pro235Leu)	rs149910292	0.00372
NM_001286577.2(C2CD3):c.3910+55A>G	rs1095424

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