Related gene-specific medical variations for Gene (Select 108660405) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056407	NM_181674.3(PPP2R2B):c.75-562AGC[9]	LOC108660405, PPP2R2B	Microsatellite (intron variant)	PPP2R2B-related disorder	GBenign
Select item 1050601	NM_181674.3(PPP2R2B):c.75-562AGC[4]	LOC108660405, PPP2R2B	Microsatellite (intron variant)	not provided	GBenign
Select item 5614	NM_181675.3(PPP2R2B):c.27CAG[(7_28)[ (p.Ser10[(7-28)])	LOC108660405, PPP2R2B	Microsatellite	Spinocerebellar ataxia type 12	GBenign

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