List of variants in gene CFHR5 reported as uncertain significance for immune system disorder

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_030787.4(CFHR5):c.646A>T (p.Asn216Tyr)	rs138834145	0.00009
NM_030787.4(CFHR5):c.707A>G (p.Asp236Gly)	rs1283689984	0.00001
NM_030787.4(CFHR5):c.1106T>G (p.Val369Gly)
NM_030787.4(CFHR5):c.1214T>A (p.Val405Glu)
NM_030787.4(CFHR5):c.647A>T (p.Asn216Ile)	rs147488267

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