Variant (rsID / SNP)

rs1460934

rs1460934 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBXO43. Location: chromosome 8, position 101,153,024. The table records no clinical significance for this variant.

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Reference-table entries

FBXO43Not classified

Variant type: synonymous_variant
Chromosome / position: 8:101153024
HGVS: NM_001029860.4,c.1458C>T,p.Ile486Ile
Allele change: Silent

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.