Variant (rsID / SNP)

rs8017682

rs8017682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHL33. Location: chromosome 14, position 20,903,778. The table records no clinical significance for this variant.

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Reference-table entries

KLHL33Not classified

Variant type: missense_variant
Chromosome / position: 14:20903778
HGVS: NM_001365790.2,c.193C>T,p.Leu65Phe
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.