Variant (rsID / SNP)

rs659366

rs659366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UCP2. Location: chromosome 11, position 73,694,754. Clinical significance in the table: risk factor.

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Reference-table entries

UCP2Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 11:73694754
Cytoband: 11q13.4
HGVS: NM_003355.2(UCP2):c.-1245G>A

Associated conditions / phenotypes

Body mass index quantitative trait locus 4

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.