List of variants in gene DCLRE1C reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.643C>T (p.Leu215=)	rs7076862	0.42876
NM_001033855.3(DCLRE1C):c.780+10C>T	rs35927251	0.17583
NM_001033855.3(DCLRE1C):c.728A>G (p.His243Arg)	rs12768894	0.14770
NM_001033855.3(DCLRE1C):c.512C>G (p.Pro171Arg)	rs35441642	0.09351
NM_001033855.3(DCLRE1C):c.781-17C>G	rs41298886	0.04519
NM_001033855.3(DCLRE1C):c.959C>G (p.Ser320Cys)	rs41298896	0.01123
NM_001033855.3(DCLRE1C):c.457G>A (p.Gly153Arg)	rs41297018	0.00940
NM_001033855.3(DCLRE1C):c.227G>C (p.Arg76Thr)	rs41296438	0.00789
NM_001033855.3(DCLRE1C):c.1893C>T (p.Pro631=)	rs41300676	0.00441
NM_001033855.3(DCLRE1C):c.1503T>C (p.Asp501=)	rs41300670	0.00272
NM_001033855.3(DCLRE1C):c.2001A>G (p.Leu667=)	rs61749163	0.00215
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.537+20C>A	rs199843069	0.00052
NM_001033855.3(DCLRE1C):c.1791C>T (p.Cys597=)	rs115421695	0.00048
NM_001033855.3(DCLRE1C):c.1894G>A (p.Glu632Lys)	rs61757205	0.00024
NM_001033855.3(DCLRE1C):c.1545A>G (p.Gly515=)	rs41300672	0.00017
NM_001033855.3(DCLRE1C):c.1435C>T (p.Leu479=)	rs764005111	0.00007
NM_001033855.3(DCLRE1C):c.1587A>C (p.Ser529=)	rs529177486	0.00001
NM_001033855.3(DCLRE1C):c.537+14G>A	rs546891508	0.00001
NM_001033855.3(DCLRE1C):c.110-17del	rs1415798169
NM_001033855.3(DCLRE1C):c.162-16dup	rs758968863
NM_001033855.3(DCLRE1C):c.465-16dup	rs1478774298
NM_001033855.3(DCLRE1C):c.918-14del	rs1333161578

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