List of variants in gene LEPR reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002303.6(LEPR):c.1835G>A (p.Arg612His)	rs144159890	0.00036
NM_002303.6(LEPR):c.1226C>A (p.Ala409Glu)	rs1446132233
NM_002303.6(LEPR):c.995-2A>G	rs2100932956

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