Variant (rsID / SNP)

rs14291

rs14291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FEZ2. Location: chromosome 2, position 36,810,586. The table records no clinical significance for this variant.

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Reference-table entries

FEZ2Not classified

Variant type: synonymous_variant
Chromosome / position: 2:36810586
HGVS: NM_001042548.2,c.402A>G,p.Thr134Thr
Allele change: Synonymous_T134T

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.