List of variants in gene MRE11 reported as benign for Hereditary cancer-predisposing syndrome

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1002C>G (p.Ser334Arg)	rs115244417	0.01348
NM_005591.4(MRE11):c.1032T>G (p.Leu344=)	rs11020793	0.00960
NM_005591.4(MRE11):c.2092A>G (p.Met698Val)	rs1805362	0.00548
NM_005591.4(MRE11):c.1475C>A (p.Ala492Asp)	rs61749249	0.00399
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.1780A>G (p.Arg594Gly)	rs576878377	0.00001
NM_005591.3:c.315-4insT
NM_005591.4(MRE11):c.1098+17T>C	rs1805365
NM_005591.4(MRE11):c.315-14dup	rs35062043
NM_005591.4(MRE11):c.315-4del	rs35062043
NM_005591.4(MRE11):c.37T>A (p.Phe13Ile)	rs149101834

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