Variant (rsID / SNP)

rs74604071

rs74604071 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHL8. Location: chromosome 4, position 88,116,518. The table records no clinical significance for this variant.

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Reference-table entries

KLHL8Not classified

Variant type: synonymous_variant
Chromosome / position: 4:88116518
HGVS: NM_001292003.2,c.174T>C,p.Leu58Leu
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.