Variant (rsID / SNP)
rs58556099
rs58556099 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT6A. Location: chromosome 12, position 52,886,461. The table records no clinical significance for this variant.
Reference-table entries
KRT6ANot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:52886461
- Cytoband
- 12q13.13
- HGVS
- NM_005554.4(KRT6A):c.512A>C (p.Asn171Thr)
- Allele change
- Missense_N171S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.