List of variants in gene CFHR3 reported as likely 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_021023.6(CFHR3):c.958C>A (p.Arg320=)	rs145280059	0.00123
NM_021023.6(CFHR3):c.805A>G (p.Ile269Val)	rs139520520	0.00112
NM_021023.6(CFHR3):c.966G>C (p.Gly322=)	rs149081467	0.00037
NM_021023.6(CFHR3):c.116G>A (p.Arg39His)	rs377742193
NM_021023.6(CFHR3):c.354C>T (p.Tyr118=)	rs144398879
NM_021023.6(CFHR3):c.613+405T>C
NM_021023.6(CFHR3):c.753A>G (p.Val251=)
NM_021023.6(CFHR3):c.796+512AATA[12]
NM_021023.6(CFHR3):c.796+772A>T
NM_021023.6(CFHR3):c.796C>T (p.His266Tyr)
NM_021023.6(CFHR3):c.797-64G>T
NM_021023.6(CFHR3):c.924A>G (p.Ala308=)
NM_021023.6(CFHR3):c.934A>G (p.Ile312Val)

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