Variant (rsID / SNP)

rs45476292

rs45476292 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UCP3. Location: chromosome 11, position 73,714,871. Clinical significance in the table: Benign.

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Reference-table entries

UCP3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:73714871
Cytoband: 11q13.4
HGVS: NM_003356.4(UCP3):c.824+1G>A
Allele change: Silent

Associated conditions / phenotypes

UCP3 POLYMORPHISM, EXON 6 SPLICE DONOR JUNCTION|Morbid 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.