List of variants in gene PCARE reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001029883.3(PCARE):c.1297C>T (p.Pro433Ser)	rs200696965	0.00044
NM_001029883.3(PCARE):c.3029G>A (p.Arg1010Gln)	rs201772623	0.00011
NM_001029883.3(PCARE):c.1968G>T (p.Arg656Ser)	rs201980758	0.00010
NM_001029883.3(PCARE):c.8G>A (p.Cys3Tyr)	rs1420546201

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