List of variants in gene combination DCLRE1C, SUV39H2 reported as likely benign

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001350965.2(DCLRE1C):c.*44C>G	rs76797003	0.00298
NM_001350965.2(DCLRE1C):c.1812C>T (p.Cys604=)	rs904972641	0.00029
NM_001193424.2(SUV39H2):c.781C>T (p.Arg261Cys)	rs375736366	0.00010
NM_001193424.2(SUV39H2):c.850-295C>G	rs978587789	0.00004
NM_001193424.2(SUV39H2):c.850-352G>A	rs148343292

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