C3554225[trait identifier] AND "Athena Diagnostics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 727197	NM_002303.6(LEPR):c.36T>C (p.His12=)	LEPR	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 8523	NM_002303.6(LEPR):c.326A>G (p.Lys109Arg)	LEPR (K109R)	Single nucleotide variant (missense variant)	Monogenic Non-Syndromic Obesity +3 more	GBenign
Select item 487357	NM_002303.6(LEPR):c.370+16G>T	LEPR	Single nucleotide variant (intron variant)	Obesity due to leptin receptor gene deficiency +1 more	GBenign
Select item 8521	NM_002303.6(LEPR):c.668A>G (p.Gln223Arg)	LEPR (Q223R)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 297991	NM_002303.6(LEPR):c.1029T>C (p.Ser343=)	LEPR	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 631614	NM_002303.6(LEPR):c.1835G>A (p.Arg612His)	LEPR (R612H)	Single nucleotide variant (missense variant)	LEPR-related disorder +2 more	GPathogenic/Likely pathogenic
Select item 8524	NM_002303.6(LEPR):c.1968G>C (p.Lys656Asn)	LEPR (K656N)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 804989	NM_002303.6(LEPR):c.2597+15G>C	LEPR	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 298000	NM_002303.6(LEPR):c.3057G>A (p.Pro1019=)	LEPR	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign

ClinVar