List of variants in gene combination DLL3, LOC130064417 reported as likely benign for Spondylocostal dysostosis 1, autosomal recessive

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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_203486.3(DLL3):c.425T>A (p.Leu142Gln)	rs55741253	0.06752
NM_203486.3(DLL3):c.618C>T (p.Pro206=)	rs192624990	0.00153
NM_203486.3(DLL3):c.616C>G (p.Pro206Ala)	rs376905666

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