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Variant (rsID / SNP)

rs1805094

LEPR

rs1805094 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LEPR. Location: chromosome 1, position 66,075,952. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LEPRBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
1:66075952
Cytoband
1p31.3
HGVS
NM_002303.6(LEPR):c.1968G>C (p.Lys656Asn)
Allele change
Missense_K656N

Associated conditions / phenotypes

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

Public references

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