List of variants in gene SETD5 reported as likely pathogenic by Revvity Omics, Revvity

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001080517.3(SETD5):c.2104-1G>T	rs2125288295
NM_001080517.3(SETD5):c.2644C>T (p.Arg882Ter)	rs1553635637
NM_001080517.3(SETD5):c.891delinsAAG (p.Ile298fs)	rs2125187739

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