ClinVar Miner

List of variants in gene combination DCLRE1C, SUV39H2 studied for Severe combined immunodeficiency due to DCLRE1C deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001193424.2(SUV39H2):c.850-305C>T	rs60006238	0.08419
NC_000010.11:g.(?_14903611)_(14955432_?)dup

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