"PreventionGenetics, part of Exact Sciences"[submitter] AND "PPP2R1B"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041075	NM_015191.3(SIK2):c.*2829T>C	PPP2R1B, SIK2	Single nucleotide variant (3 prime UTR variant)	PPP2R1B-related disorder	GLikely benign
Select item 3039930	NM_015191.3(SIK2):c.*2840T>A	SIK2, PPP2R1B (D603V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	PPP2R1B-related disorder	GLikely benign
Select item 2642364	NM_181700.2(PPP2R1B):c.1675A>T (p.Asn559Tyr)	PPP2R1B (N559Y +1 more)	Single nucleotide variant (missense variant)	PPP2R1B-related disorder +1 more	GBenign/Likely benign
Select item 3057072	NM_181700.2(PPP2R1B):c.1633G>C (p.Val545Leu)	PPP2R1B (V545L +1 more)	Single nucleotide variant (missense variant)	PPP2R1B-related disorder	GBenign
Select item 3034260	NM_002716.5(PPP2R1B):c.1783A>G (p.Ile595Val)	PPP2R1B (I468V +3 more)	Single nucleotide variant (missense variant)	PPP2R1B-related disorder	GLikely benign
Select item 3051639	NM_002716.5(PPP2R1B):c.1697+8T>G	PPP2R1B	Single nucleotide variant (intron variant)	PPP2R1B-related disorder	GLikely benign

ClinVar