Variant (rsID / SNP)

rs1055741

rs1055741 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBXO16. Location: chromosome 8, position 28,286,174. The table records no clinical significance for this variant.

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Reference-table entries

FBXO16Not classified

Variant type: 3_prime_UTR_variant
Chromosome / position: 8:28286174
HGVS: NM_172366.4,c.*70A>C
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.