List of variants in gene combination MIR3661, PPP2CA reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002715.4(PPP2CA):c.100_102del (p.Lys34del)	rs2149390312
NM_002715.4(PPP2CA):c.10_12del (p.Lys4del)	rs2149390364
NM_002715.4(PPP2CA):c.35A>T (p.Gln12Leu)
NM_002715.4(PPP2CA):c.41T>C (p.Ile14Thr)	rs2481101927
NM_002715.4(PPP2CA):c.61A>G (p.Lys21Glu)	rs1461847477
NM_002715.4(PPP2CA):c.71C>T (p.Ser24Phe)
NM_002715.4(PPP2CA):c.77C>T (p.Ser26Phe)	rs772521505

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