List of variants in gene CHD5 reported as uncertain significance 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_015557.3(CHD5):c.5249C>T (p.Thr1750Met)	rs139581412	0.00064
NM_015557.3(CHD5):c.5305A>G (p.Asn1769Asp)	rs754161216	0.00001
NM_015557.3(CHD5):c.3680G>C (p.Gly1227Ala)	rs1557544846

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