ClinVar Miner

List of variants in gene CD3E reported as likely benign for Severe combined immunodeficiency disease

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000733.4(CD3E):c.507C>T (p.Gly169=)	rs2231447	0.00816
NM_000733.4(CD3E):c.498G>A (p.Ala166=)	rs78373007	0.00262

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