Variant (rsID / SNP)

rs8113389

rs8113389 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBXO17. Location: chromosome 19, position 39,433,299. The table records no clinical significance for this variant.

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Reference-table entries

FBXO17Not classified

Variant type: synonymous_variant
Chromosome / position: 19:39433299
HGVS: NM_148169.3,c.813T>C,p.Tyr271Tyr
Allele change: Synonymous_Y271Y

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.