Variant (rsID / SNP)

rs121909065

rs121909065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CARTPT. Location: chromosome 5, position 71,015,730. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CARTPTUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 5:71015730
Cytoband: 5q13.2
HGVS: NM_004291.4(CARTPT):c.183G>C (p.Leu61Phe)
Allele change: Missense_L61F

Associated conditions / phenotypes

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.