List of variants in gene LYSET reported as pathogenic for bone development disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001098621.4(LYSET):c.115C>T (p.Arg39Trp)	rs2140085425
NM_001098621.4(LYSET):c.197dup (p.Tyr66Ter)	rs1291335611

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