Variant (rsID / SNP)

rs371789455

rs371789455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UCP2. Location: chromosome 11, position 73,687,954. Clinical significance in the table: Likely benign.

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Reference-table entries

UCP2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:73687954
Cytoband: 11q13.4
HGVS: NM_003355.3(UCP2):c.446G>A (p.Arg149Gln)
Allele change: Missense_R149Q

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.