ClinVar Miner

List of variants in gene LEPR, LOC122094844 studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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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.2034A>T (p.Arg678Ser)	rs377399607
NM_002303.6(LEPR):c.2063A>G (p.Asn688Ser)	rs1657507283

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