List of variants in gene PDZD4 reported as likely benign by Ambry Genetics

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_001303512.2(PDZD4):c.2269G>A (p.Ala757Thr)	rs968113390	0.00003
NM_001303512.2(PDZD4):c.1349C>G (p.Ala450Gly)	rs782291507	0.00001
NM_001303512.2(PDZD4):c.1354A>G (p.Ser452Gly)	rs2520595804
NM_001303512.2(PDZD4):c.1559C>A (p.Pro520His)

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