ClinVar Miner

List of variants in gene combination DCLRE1C, SUV39H2 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001350965.2(DCLRE1C):c.1812C>T (p.Cys604=)	rs904972641	0.00029
NM_001193424.2(SUV39H2):c.850-295C>G	rs978587789	0.00004

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