List of variants in gene NEU1 reported as benign for not provided

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000434.4(NEU1):c.263G>C (p.Gly88Ala)	rs34712643	0.02415
NM_000434.4(NEU1):c.1239G>A (p.Gly413=)	rs114618932	0.00093
NM_000434.4(NEU1):c.486C>T (p.Ala162=)	rs115588976	0.00026
NM_000434.4(NEU1):c.1021+15G>C	rs567907055	0.00004
NM_000434.4(NEU1):c.*210T>A	rs13118

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