ClinVar Miner

List of variants in gene DCLRE1C reported as benign for DCLRE1C-related disorder

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.1894G>A (p.Glu632Lys)	rs61757205	0.00024
NM_001033855.3(DCLRE1C):c.1545A>G (p.Gly515=)	rs41300672	0.00017

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