Variant (rsID / SNP)

rs1805096

rs1805096 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LEPR. Location: chromosome 1, position 66,102,257. Clinical significance in the table: Benign.

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Reference-table entries

LEPRBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:66102257
Cytoband: 1p31.3
HGVS: NM_002303.6(LEPR):c.3057G>A (p.Pro1019=)
Allele change: Synonymous_P1019P

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.