List of variants in gene C5AR1 reported as uncertain significance 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)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001736.4(C5AR1):c.316G>A (p.Gly106Arg)	rs750171124	0.00004
NM_001736.4(C5AR1):c.100C>T (p.Arg34Cys)	rs774370669	0.00003
NM_001736.4(C5AR1):c.532C>T (p.Arg178Trp)	rs750580655	0.00002
NM_001736.4(C5AR1):c.509C>A (p.Pro170His)	rs2514890152
NM_001736.4(C5AR1):c.936del (p.Lys313fs)	rs2514890878

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