ClinVar Miner

List of variants in gene MRE11 reported as likely pathogenic by GeneDx

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1015A>T (p.Lys339Ter)	rs984874083	0.00004
NM_005591.4(MRE11):c.845+6T>G	rs2135045937

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