ClinVar Miner

List of variants in gene CD3D reported as uncertain significance 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_000732.6(CD3D):c.450+6C>T	rs193922617	0.00013
NM_000732.6(CD3D):c.-37G>T	rs886047738

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