ClinVar Miner

List of variants reported as likely pathogenic for Intellectual disability, autosomal recessive 34 by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003805.5(CRADD):c.285dup (p.Asp96fs)	rs1555213545
NM_003805.5(CRADD):c.393G>A (p.Trp131Ter)	rs2540635374
NM_003805.5(CRADD):c.50del (p.Gly17fs)	rs1207931375

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