List of variants in gene CFHR3 reported as uncertain significance for inherited retinal dystrophy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_021023.6(CFHR3):c.534A>T (p.Gly178=)
NM_021023.6(CFHR3):c.839_840del (p.Ile280fs)	rs781400776
NM_021023.6(CFHR3):c.99_105del (p.Phe34fs)

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