List of variants in gene DCLRE1C reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.1893C>T (p.Pro631=)	rs41300676	0.00441
NM_001033855.3(DCLRE1C):c.1008C>T (p.Asn336=)	rs115524993	0.00209
NM_001033855.3(DCLRE1C):c.36A>C (p.Pro12=)	rs148108773	0.00113
NM_001033855.3(DCLRE1C):c.1101A>G (p.Pro367=)	rs143782439	0.00085
NM_001033855.3(DCLRE1C):c.973-1801T>A	rs557886549	0.00027
NM_001033855.3(DCLRE1C):c.741A>G (p.Thr247=)	rs369844484	0.00007
NM_001033855.3(DCLRE1C):c.1800T>C (p.Asp600=)	rs199619187	0.00004
NM_001033855.3(DCLRE1C):c.537+14G>A	rs546891508	0.00001
NM_001033855.3(DCLRE1C):c.918-14del	rs1333161578

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