List of variants in gene MRE11 reported as benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.20+28G>A	rs497763	0.42216
NM_005591.4(MRE11):c.1225+19T>C	rs641936	0.36577
NM_005591.4(MRE11):c.403-6G>A	rs535801	0.28996
NM_005591.4(MRE11):c.1032T>G (p.Leu344=)	rs11020793	0.00960
NM_005591.4(MRE11):c.771A>G (p.Glu257=)	rs13447632	0.00301
NM_005591.4(MRE11):c.1783+5G>C	rs142082313	0.00284
NM_005591.4(MRE11):c.845+11T>C	rs140145979	0.00021
NM_005591.4(MRE11):c.1780A>G (p.Arg594Gly)	rs576878377	0.00001
NM_005591.4(MRE11):c.1098+17T>C	rs1805365
NM_005591.4(MRE11):c.37T>A (p.Phe13Ile)	rs149101834

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