Variant (rsID / SNP)

rs4624233

rs4624233 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT28. Location: chromosome 17, position 38,955,961. The table records no clinical significance for this variant.

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Reference-table entries

KRT28Not classified

Variant type: missense_variant
Chromosome / position: 17:38955961
HGVS: NM_181535.3,c.185C>T,p.Ala62Val
Allele change: Missense_A62V

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.