List of variants in gene MRE11 reported as likely benign by Sema4, Sema4

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1783+5G>C	rs142082313	0.00284
NM_005591.4(MRE11):c.969A>G (p.Pro323=)	rs13447633	0.00258
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.120C>T (p.Leu40=)	rs1805364	0.00066
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.777G>A (p.Gln259=)	rs774144789	0.00006
NM_005591.4(MRE11):c.81G>A (p.Glu27=)	rs190031653	0.00006
NM_005591.4(MRE11):c.2049G>A (p.Gly683=)	rs758931835	0.00004
NM_005591.4(MRE11):c.180T>C (p.Asp60=)	rs1213393080	0.00001
NM_005591.4(MRE11):c.33C>T (p.Asn11=)	rs746088302	0.00001
NM_005591.4(MRE11):c.1089A>G (p.Val363=)	rs786201824
NM_005591.4(MRE11):c.1564-15TCT[4]	rs761058908
NM_005591.4(MRE11):c.2007A>G (p.Thr669=)	rs1554999945
NM_005591.4(MRE11):c.2079T>C (p.Asp693=)	rs1354524779
NM_005591.4(MRE11):c.315-5_315-4dup	rs35062043
NM_005591.4(MRE11):c.37T>A (p.Phe13Ile)	rs149101834

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