List of variants in gene CFB reported as uncertain significance for age-related macular degeneration

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_001710.6(CFB):c.658+7T>C	rs541260302	0.00049
NM_001710.6(CFB):c.1374G>A (p.Met458Ile)	rs200837114	0.00004
NM_001710.6(CFB):c.-3G>A	rs755016493	0.00003

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