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Variant (rsID / SNP)

rs10852985

ANKFN1

rs10852985 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKFN1. Location: chromosome 17, position 54,534,634. The table records no clinical significance for this variant.

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Reference-table entries

ANKFN1Not classified
Variant type
missense_variant
Chromosome / position
17:54534634
HGVS
NM_001370326.1,c.1324G>A,p.Val442Ile
Allele change
Missense_V445I

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.