ClinVar Miner

List of variants in gene C5AR1 reported as likely benign for C5AR1-related disorder

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001736.4(C5AR1):c.657G>A (p.Thr219=)	rs117536261	0.00030
NM_001736.4(C5AR1):c.813G>A (p.Ser271=)	rs948785923	0.00002

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