List of variants in gene CFHR5 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_030787.4(CFHR5):c.1704T>A (p.Cys568Ter)	rs143140599	0.00764
NM_030787.4(CFHR5):c.832G>A (p.Gly278Ser)	rs139017763	0.00689
NM_030787.4(CFHR5):c.429T>C (p.Thr143=)	rs140215003	0.00608
NM_030787.4(CFHR5):c.254-5C>T	rs185709089	0.00368
NM_030787.4(CFHR5):c.432A>T (p.Lys144Asn)	rs181511327	0.00076
NM_030787.4(CFHR5):c.232T>C (p.Ser78Pro)	rs146025130	0.00046
NM_030787.4(CFHR5):c.533A>G (p.Asn178Ser)	rs200427185	0.00013
NM_030787.4(CFHR5):c.1304G>A (p.Arg435Gln)	rs776538115	0.00005
NM_030787.4(CFHR5):c.826G>A (p.Glu276Lys)	rs199531514	0.00001

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.