Variant (rsID / SNP)
rs665470
rs665470 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT71. Location: chromosome 12, position 52,946,498. The table records no clinical significance for this variant.
Reference-table entries
KRT71Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:52946498
- HGVS
- NM_033448.3,c.364G>A,p.Glu122Lys
- Allele change
- Missense_E122K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.