List of variants in gene CHD2 studied for Autism spectrum disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001271.4(CHD2):c.5134C>T (p.His1712Tyr)	rs1006465697	0.00001
NM_001271.4(CHD2):c.3427T>G (p.Tyr1143Asp)	rs2505576939
NM_001271.4(CHD2):c.5474T>G (p.Val1825Gly)	rs2505651204
NM_001271.4(CHD2):c.995_999del (p.Val332fs)	rs2505447123

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