List of variants reported as benign for Lafora disease

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_005670.4(EPM2A):c.159C>G (p.Ala53=)	rs2235482	0.63686
NM_198586.3(NHLRC1):c.332C>T (p.Pro111Leu)	rs10949483	0.35277
NM_005670.4(EPM2A):c.402G>A (p.Gly134=)	rs35230590	0.18342
NM_198586.3(NHLRC1):c.312T>C (p.His104=)	rs115931931	0.10897
NM_198586.3(NHLRC1):c.*621T>A	rs10949481	0.08640
NM_198586.3(NHLRC1):c.*336G>A	rs10949482	0.06918
NM_198586.3(NHLRC1):c.*626C>T	rs10949480	0.06100
NM_198586.3(NHLRC1):c.*237T>C	rs73379118	0.01527
NM_198586.3(NHLRC1):c.*85T>A	rs73379121	0.01526
NM_198586.3(NHLRC1):c.*276G>C	rs11966748	0.01453
NM_198586.3(NHLRC1):c.*344A>T	rs147528518	0.00663
NM_198586.3(NHLRC1):c.303G>T (p.Pro101=)	rs187783545	0.00443
NM_198586.3(NHLRC1):c.32C>A (p.Ala11Glu)	rs139029314	0.00181
NM_198586.3(NHLRC1):c.*886G>A	rs146342540	0.00093
NM_198586.3(NHLRC1):c.969C>T (p.Ser323=)	rs142941035	0.00022
NM_198586.3(NHLRC1):c.504G>T (p.Gly168=)	rs529490452	0.00001
NM_198586.3(NHLRC1):c.*482C>G	rs114713758
NM_198586.3(NHLRC1):c.*55G>C	rs11966789

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