C3554689[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 159722	NM_181523.3(PIK3R1):c.219C>T (p.Tyr73=)	PIK3R1	Single nucleotide variant (synonymous variant)	Agammaglobulinemia 7, autosomal recessive +4 more	GBenign/Likely benign
Select item 159723	NM_181523.3(PIK3R1):c.334+14A>C	PIK3R1	Single nucleotide variant (intron variant)	Agammaglobulinemia 7, autosomal recessive +4 more	GBenign/Likely benign
Select item 1271646	NM_181523.3(PIK3R1):c.428-21G>A	PIK3R1	Single nucleotide variant (intron variant)	Immunodeficiency 36 +4 more	GBenign

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