List of variants in gene CRADD reported as 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: 5

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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.382G>C (p.Gly128Arg)	rs387906861	0.00005
NM_003805.5(CRADD):c.491T>G (p.Phe164Cys)	rs370916968	0.00003
NM_003805.5(CRADD):c.508C>T (p.Arg170Cys)	rs749655461	0.00001
NM_003805.5(CRADD):c.393G>A (p.Trp131Ter)

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