Variant (rsID / SNP)

rs1051489

rs1051489 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFR. Location: chromosome 5, position 32,400,266. The table records no clinical significance for this variant.

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Reference-table entries

ZFRNot classified

Variant type: missense_variant
Chromosome / position: 5:32400266
HGVS: NM_016107.5,c.1559T>C,p.Ile520Thr
Allele change: Missense_I520T

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.