List of variants in gene SETD5 reported as pathogenic for Intellectual disability

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.2177_2178del (p.Thr726fs)	rs587777326
NM_001080517.3(SETD5):c.2347-7A>G	rs886041593
NM_001080517.3(SETD5):c.648del (p.Gln216fs)	rs2041147607

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