Variant (rsID / SNP)

rs3742569

rs3742569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBXO34. Location: chromosome 14, position 55,818,706. The table records no clinical significance for this variant.

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Reference-table entries

FBXO34Not classified

Variant type: missense_variant
Chromosome / position: 14:55818706
HGVS: NM_017943.4,c.1598T>C,p.Leu533Pro
Allele change: Missense_L533P

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.