List of variants in gene CP reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000096.4(CP):c.1099C>T (p.Arg367Cys)	rs34624984	0.01447
NM_000096.4(CP):c.2522C>G (p.Thr841Arg)	rs56033670	0.00435
NM_000096.4(CP):c.2571C>T (p.Tyr857=)	rs151304828	0.00189
NM_000096.4(CP):c.944A>G (p.Asn315Ser)	rs370682704	0.00017
NM_000096.4(CP):c.1493A>G (p.Gln498Arg)	rs17847018	0.00011
NM_000096.4(CP):c.828T>C (p.Cys276=)	rs781181406	0.00003

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