Variant (rsID / SNP)
rs11170177
rs11170177 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT74. Location: chromosome 12, position 52,966,428. The table records no clinical significance for this variant.
Reference-table entries
KRT74Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:52966428
- HGVS
- NM_175053.4,c.495C>G,p.Asn165Lys
- Allele change
- Missense_N165K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.