List of variants in gene CHD2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001271.4(CHD2):c.2049A>G (p.Glu683=)	rs4777755	0.77324
NM_001271.4(CHD2):c.2718A>G (p.Gln906=)	rs11074121	0.75493
NM_001271.4(CHD2):c.5416A>C (p.Arg1806=)	rs12906163	0.28315
NM_001271.4(CHD2):c.3564C>T (p.Tyr1188=)	rs2272457	0.23362
NM_001271.4(CHD2):c.4527C>T (p.Ile1509=)	rs34315566	0.04350
NM_001271.4(CHD2):c.4721G>C (p.Gly1574Ala)	rs56227200	0.02390
NM_001271.4(CHD2):c.3596-20G>A	rs78359469	0.02014
NM_001271.4(CHD2):c.3540C>T (p.Ser1180=)	rs76621355	0.00866
NM_001271.4(CHD2):c.693-20C>T	rs141271290	0.00778
NM_001271.4(CHD2):c.1788T>C (p.Tyr596=)	rs144093014	0.00698
NM_001271.4(CHD2):c.2577+7T>C	rs146944583	0.00371
NM_001271.4(CHD2):c.4138-6T>C	rs182330071	0.00325
NM_001271.4(CHD2):c.608A>G (p.Lys203Arg)	rs117844037	0.00256
NM_001271.4(CHD2):c.330G>A (p.Arg110=)	rs138626801	0.00140
NM_001271.4(CHD2):c.3400G>A (p.Ala1134Thr)	rs147466101	0.00023
NM_001271.4(CHD2):c.3126C>T (p.Asp1042=)	rs150268140

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