List of variants in gene CRADD reported as likely pathogenic for autosomal recessive non-syndromic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003805.5(CRADD):c.509G>A (p.Arg170His)	rs141179774	0.00053
NM_003805.5(CRADD):c.285dup (p.Asp96fs)	rs1555213545
NM_003805.5(CRADD):c.393G>A (p.Trp131Ter)
NM_003805.5(CRADD):c.50del (p.Gly17fs)	rs1207931375

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