Variant (rsID / SNP)

rs16139

rs16139 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPY. Location: chromosome 7, position 24,324,879. Clinical significance in the table: Benign.

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Reference-table entries

NPYBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:24324879
Cytoband: 7p15.3
HGVS: NM_000905.4(NPY):c.20T>C (p.Leu7Pro)
Allele change: Missense_L7P

Associated conditions / phenotypes

NEUROPEPTIDE Y POLYMORPHISM

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.