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Variant (rsID / SNP)

rs61781316

LEPR

rs61781316 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LEPR. Location: chromosome 1, position 66,102,617. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LEPRConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:66102617
Cytoband
1p31.3
HGVS
NM_002303.6(LEPR):c.3417A>G (p.Ala1139=)
Allele change
Synonymous_A1139A

Associated conditions / phenotypes

Obesity|Obesity due to leptin receptor gene deficiency|Monogenic Non-Syndromic Obesity

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.