"GeneDx"[submitter] AND "PYY"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 59586	GRCh38/hg38 17q21.31(chr17:43570878-44762377)x1	ADAM11, ASB16 +104 more	Copy number loss	See cases	GPathogenic
Select item 1249578	NM_001394028.1(PYY):c.*149C>A	PYY	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1243115	NM_001394028.1(PYY):c.270-61C>T	PYY	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 768889	NM_001394028.1(PYY):c.218T>C (p.Leu73Pro)	PYY (L73P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1178202	NM_001394028.1(PYY):c.215C>G (p.Thr72Arg)	PYY (T72R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1266712	NM_004160.6(PYY):c.-463+3069G>T	PYY	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221561	NM_004160.6(PYY):c.-463+2881_-463+2883del	PYY	Microsatellite (intron variant)	not provided	GBenign
Select item 1231148	NM_004160.6(PYY):c.-463+2622_-463+2623insC	PYY	Insertion (intron variant)	not provided	GBenign

ClinVar