List of variants in gene combination C2, CFB reported as likely benign for age-related macular degeneration

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001710.5(CFB):c.94C>T (p.Arg32Trp)	rs12614	0.17324
NM_001710.6(CFB):c.1137C>T (p.Arg379=)	rs45600936	0.00911
NM_000063.6(C2):c.2046A>G (p.Ala682=)	rs45507391	0.00154
NM_000063.6(C2):c.1778G>A (p.Arg593Gln)	rs150878060	0.00133
NM_000063.6(C2):c.1414G>A (p.Ala472Thr)	rs142243595	0.00105
NM_000063.6(C2):c.*304A>G	rs72842444	0.00006
NM_000063.6(C2):c.1529G>A (p.Arg510His)	rs45476300	0.00006
NM_000063.6(C2):c.1835G>A (p.Ser612Asn)	rs573509224	0.00001

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