Related gene-specific medical variations for Gene (Select 644997) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2638189	NM_005026.5(PIK3CD):c.-138+2505G>A	PIK3CD, PIK3CD-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2638188	NM_005026.5(PIK3CD):c.-138+2480C>T	PIK3CD, PIK3CD-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 982099	NM_005026.5(PIK3CD):c.-138+2682G>C	PIK3CD, PIK3CD-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +1 more	GBenign/Likely benign

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