List of variants in gene PRPF3 reported as benign for Retinal dystrophy

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004698.4(PRPF3):c.1407G>A (p.Met469Ile)	rs587594838	0.00011
NM_004698.4(PRPF3):c.2019G>A (p.Ala673=)	rs189302002	0.00006
NM_004698.4(PRPF3):c.1897G>C (p.Val633Leu)	rs141881079	0.00004

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