Variant (rsID / SNP)
rs17558560
rs17558560 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT27. Location: chromosome 17, position 38,936,659. The table records no clinical significance for this variant.
Reference-table entries
KRT27Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:38936659
- HGVS
- NM_181537.4,c.577G>A,p.Gly193Ser
- Allele change
- Missense_G193S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.