ClinVar Miner

List of variants in gene DCLRE1C reported as 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_001033855.3(DCLRE1C):c.643C>T (p.Leu215=)	rs7076862	0.42876
NM_001033855.3(DCLRE1C):c.512C>G (p.Pro171Arg)	rs35441642	0.09351

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