List of variants in gene ADAM22 reported as pathogenic for complex neurodevelopmental disorder

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_001324418.2(ADAM22):c.1202G>A (p.Cys401Tyr)	rs747259064	0.00001
NM_001324418.2(ADAM22):c.2396del (p.Ser799fs)	rs1554519462
NM_001324418.2(ADAM22):c.2860C>T (p.Arg954Ter)	rs1262642807
NM_001324418.2(ADAM22):c.2888C>T (p.Ser963Phe)

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