List of variants in gene DCLRE1C reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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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.161+119A>G	rs41304332	0.01092
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.1008C>T (p.Asn336=)	rs115524993	0.00209

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