List of variants in gene NMNAT1 reported as benign for retinal disorder

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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_022787.4(NMNAT1):c.115+3A>G	rs181504239	0.00447
NM_022787.4(NMNAT1):c.440-16G>T	rs181513024	0.00353
NM_022787.4(NMNAT1):c.23A>C (p.Glu8Ala)	rs61740429	0.00103
NM_022787.4(NMNAT1):c.764G>A (p.Ser255Asn)	rs138626416	0.00024
NM_022787.4(NMNAT1):c.471A>G (p.Ala157=)	rs373788044	0.00001

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