Variant (rsID / SNP)

rs13306523

rs13306523 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LEPROT, LEPR. Location: chromosome 1, position 65,890,990. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LEPROTConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 1:65890990
Cytoband: 1p31.3
HGVS: NM_002303.6(LEPR):c.-92C>T
Allele change: Synonymous_L7L

Associated conditions / phenotypes

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

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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