List of variants in gene combination LOC126805613, NMNAT1 reported as likely pathogenic for NMNAT1-related retinopathy

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022787.4(NMNAT1):c.-72G>A	rs1475372376	0.00001
NM_022787.4(NMNAT1):c.-57+10C>T	rs1640875786
NM_022787.4(NMNAT1):c.-57+4A>G	rs957312118
NM_022787.4(NMNAT1):c.-57G>T	rs1640875002

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