List of variants in gene NEFL reported as benign for not provided

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006158.3(NEFL):c.-374A>G	rs2979687	0.59042
NM_006158.4(NEFL):c.-176C>A	rs2979688	0.53692
NM_006158.5(NEFL):c.1044+39G>C	rs6982740	0.07439
NM_006158.5(NEFL):c.667C>T (p.Leu223=)	rs60156239	0.00494
NM_006158.5(NEFL):c.1275C>T (p.Gly425=)	rs114329068	0.00395
NM_006158.5(NEFL):c.1402G>A (p.Asp468Asn)	rs57153321	0.00081
NM_006158.5(NEFL):c.1458C>T (p.Ala486=)	rs61726486	0.00007
NM_006158.5(NEFL):c.*235A>T	rs1059111
NM_006158.5(NEFL):c.289C>T (p.Leu97Phe)	rs587777888
NM_006158.5(NEFL):c.338_339delinsCC (p.Gln113Pro)	rs1554497641

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