Variant (rsID / SNP)

rs758033

rs758033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AXIN1. Location: chromosome 16, position 397,044. The table records no clinical significance for this variant.

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Reference-table entries

AXIN1Not classified

Variant type: 5_prime_UTR_variant
Chromosome / position: 16:397044
HGVS: NM_003502.4,c.-19C>A
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.