List of variants in gene combination DCLRE1C, SUV39H2 reported as uncertain significance for not specified

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001193424.2(SUV39H2):c.899A>G (p.Lys300Arg)	rs1212027801	0.00001
NM_001193424.2(SUV39H2):c.1022A>T (p.Asn341Ile)
NM_001193424.2(SUV39H2):c.1139T>C (p.Ile380Thr)
NM_001193424.2(SUV39H2):c.1159C>G (p.His387Asp)	rs2491559996
NM_001193424.2(SUV39H2):c.719C>G (p.Pro240Arg)

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