List of variants in gene DCLRE1C reported as likely pathogenic 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)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.1265C>G (p.Ser422Ter)	rs1354336544
NM_001033855.3(DCLRE1C):c.247-1G>C	rs2131027668
NM_001033855.3(DCLRE1C):c.406G>A (p.Asp136Asn)	rs1839765652
NM_001033855.3(DCLRE1C):c.95C>T (p.Ser32Phe)	rs969498121

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