ClinVar Miner

List of variants in gene PIDD1 reported as likely pathogenic for Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly

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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_145886.4(PIDD1):c.2042-2A>G	rs199752248	0.00009
NM_145886.4(PIDD1):c.296-1G>A	rs1479635413	0.00001
NM_145886.4(PIDD1):c.1302+1G>A

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