Variant (rsID / SNP)

rs10803354

rs10803354 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KAZN. Location: chromosome 1, position 15,438,990. The table records no clinical significance for this variant.

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Reference-table entries

KAZNNot classified

Variant type: missense_variant
Chromosome / position: 1:15438990
HGVS: NM_201628.3,c.2116G>A,p.Ala706Thr
Allele change: Missense_A706T

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.