Variants in gene MRE11 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1475C>A (p.Ala492Asp)	rs61749249	0.00399
NM_005591.4(MRE11):c.1783+5G>C	rs142082313	0.00284
NM_005591.4(MRE11):c.822T>C (p.Leu274=)	rs137868143	0.00152
NM_005591.4(MRE11):c.426C>T (p.Asp142=)	rs3218740	0.00109
NM_005591.4(MRE11):c.1798G>C (p.Glu600Gln)	rs145415033	0.00103
NM_005591.4(MRE11):c.1727G>A (p.Arg576Gln)	rs139461096	0.00038
NM_005591.4(MRE11):c.1480G>A (p.Glu494Lys)	rs104895016	0.00032
NM_005591.4(MRE11):c.1491C>T (p.Ile497=)	rs199634245	0.00021
NM_005591.4(MRE11):c.1090C>A (p.Arg364=)	rs371077728

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