List of variants in gene MRE11 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1783+5G>C	rs142082313	0.00284
NM_005591.4(MRE11):c.1286T>C (p.Val429Ala)	rs141293060	0.00023
NM_005591.4(MRE11):c.1643T>C (p.Ile548Thr)	rs373522639	0.00016
NM_005591.4(MRE11):c.1504C>T (p.Arg502Cys)	rs186333183	0.00015
NM_005591.4(MRE11):c.534A>G (p.Leu178=)	rs374635285	0.00003
NM_005591.4(MRE11):c.1098+10A>G	rs1946604458	0.00001
NM_005591.4(MRE11):c.1476C>T (p.Ala492=)	rs370397034	0.00001
NM_005591.4(MRE11):c.19C>T (p.Leu7Phe)	rs73517551
NM_005591.4(MRE11):c.2007A>G (p.Thr669=)	rs1554999945
NM_005591.4(MRE11):c.235T>C (p.Leu79=)	rs745332888
NM_005591.4(MRE11):c.573A>C (p.Arg191=)	rs1555014571

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