List of variants in gene NAA15 reported as likely pathogenic for 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_057175.5(NAA15):c.1410+1G>T	rs1553996876
NM_057175.5(NAA15):c.1841del (p.Asn614fs)	rs1283385686
NM_057175.5(NAA15):c.218T>C (p.Leu73Ser)	rs2110902008

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