List of variants in gene combination LEPR, LOC122094844 reported as uncertain significance for Obesity due to leptin receptor gene deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002303.6(LEPR):c.2171T>C (p.Val724Ala)	rs375934938	0.00009
NM_002303.6(LEPR):c.2185T>G (p.Leu729Val)	rs768503592	0.00003
NM_002303.6(LEPR):c.2046C>T (p.Asn682=)	rs192825082	0.00001
NM_002303.6(LEPR):c.2103C>T (p.Phe701=)	rs755504289	0.00001

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