ClinVar Miner

List of variants in gene DCLRE1C reported by Neuberg Centre For Genomic Medicine, NCGM

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_001033855.3(DCLRE1C):c.1333C>T (p.Arg445Cys)	rs774273800	0.00001
NM_001033855.3(DCLRE1C):c.679-1G>A	rs2130918080

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