Variant (rsID / SNP)

rs874889

rs874889 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT24. Location: chromosome 17, position 38,857,446. The table records no clinical significance for this variant.

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Reference-table entries

KRT24Not classified

Variant type: missense_variant
Chromosome / position: 17:38857446
HGVS: NM_019016.3,c.801G>T,p.Met267Ile
Allele change: Missense_M267I

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.