List of variants in gene MRE11 reported as not provided by Harris Lab, University of Minnesota

Minimum submission review status:		Collection method:
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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1099-217A>G	rs104895017	0.01545
NM_005591.4(MRE11):c.1475C>A (p.Ala492Asp)	rs61749249	0.00399
NM_005591.4(MRE11):c.21-100T>A	rs104895020	0.00236
NM_005591.4(MRE11):c.1995-94G>A	rs104895012	0.00150
NM_005591.4(MRE11):c.1995-111G>T	rs104895013	0.00123
NM_005591.4(MRE11):c.1480G>A (p.Glu494Lys)	rs104895016	0.00032
NM_005591.4(MRE11):c.*656T>C	rs104895009	0.00009
NM_005591.4(MRE11):c.*1228A>G	rs104895007
NM_005591.4(MRE11):c.*1746G>T	rs104895006
NM_005591.4(MRE11):c.*1776C>T	rs104895005
NM_005591.4(MRE11):c.*1933G>T	rs104895004
NM_005591.4(MRE11):c.*214T>G	rs104895011
NM_005591.4(MRE11):c.*431G>T	rs104895010
NM_005591.4(MRE11):c.*685C>T	rs104895008
NM_005591.4(MRE11):c.1098+131A>C	rs104895018
NM_005591.4(MRE11):c.1500+168A>G	rs104895015
NM_005591.4(MRE11):c.1784-116C>G	rs104895014
NM_005591.4(MRE11):c.845+86G>A	rs104895019

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