List of variants in gene CFI reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_000204.5(CFI):c.1534+5G>T	rs114013791	0.00951
NM_000204.5(CFI):c.1206C>T (p.Pro402=)	rs115780371	0.00646
NM_000204.5(CFI):c.1443C>T (p.Val481=)	rs114091883	0.00190
NM_000204.5(CFI):c.782G>A (p.Gly261Asp)	rs112534524	0.00153
NM_000204.5(CFI):c.319A>G (p.Thr107Ala)	rs201419000	0.00036
NM_000204.5(CFI):c.429C>T (p.Ser143=)	rs112492491	0.00034
NM_000204.5(CFI):c.1430-19G>A	rs377117137	0.00019
NM_000204.5(CFI):c.1581C>T (p.Gly527=)	rs181378677	0.00015
NM_000204.5(CFI):c.705T>C (p.Ile235=)	rs373891906	0.00010
NM_000204.5(CFI):c.482+7G>A	rs765922749	0.00006
NM_000204.5(CFI):c.1044+8C>T	rs190420174	0.00005
NM_000204.5(CFI):c.729T>A (p.Gly243=)	rs749140698	0.00005
NM_000204.5(CFI):c.1429+8T>C	rs184313022	0.00003
NM_000204.5(CFI):c.1378C>T (p.Leu460=)	rs1026187949	0.00002
NM_000204.5(CFI):c.546A>G (p.Leu182=)	rs992376160	0.00002
NM_000204.5(CFI):c.12T>A (p.Leu4=)	rs777304665	0.00001
NM_000204.5(CFI):c.1656A>G (p.Lys552=)	rs1308386684	0.00001
NM_000204.5(CFI):c.540A>G (p.Glu180=)	rs759777516	0.00001
NM_000204.5(CFI):c.192G>C (p.Pro64=)	rs571265769
NM_000204.5(CFI):c.329-14dup	rs754551276

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