ClinVar Miner

List of variants in gene NMNAT1 reported as benign for Leber congenital amaurosis 9

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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NM_022787.4(NMNAT1):c.115+3A>G rs181504239
NM_022787.4(NMNAT1):c.23A>C (p.Glu8Ala)
NM_022787.4(NMNAT1):c.471A>G (p.Ala157=)
NM_022787.4(NMNAT1):c.764G>A (p.Ser255Asn)

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