ClinVar Miner

List of variants in gene DCLRE1C reported as pathogenic for Severe combined immunodeficiency, partial

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
DCLRE1C, 17-BP DEL
NM_001033855.3(DCLRE1C):c.1350_1356del (p.Asp451fs)	rs786200884

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