Variant (rsID / SNP)

rs2167270

rs2167270 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LEP. Location: chromosome 7, position 127,881,349. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LEPBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:127881349
Cytoband: 7q32.1
HGVS: NM_000230.3(LEP):c.-39G>A
Allele change: Silent

Associated conditions / phenotypes

Obesity due to congenital leptin 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.