List of variants in gene CFH reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000186.4(CFH):c.3148A>T (p.Asn1050Tyr)	rs35274867	0.01924
NM_000186.4(CFH):c.245-7G>A	rs35814900	0.01517
NM_000186.4(CFH):c.2634C>T (p.His878=)	rs35292876	0.00829
NM_000186.4(CFH):c.3310+113A>G	rs186009355	0.00180
NC_000001.11:g.196651811C>T	rs74842824

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