Variant (rsID / SNP)
rs61735165
rs61735165 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT12. Location: chromosome 17, position 39,021,137. Clinical significance in the table: Likely_benign.
Reference-table entries
KRT12Likely benign
- Clinical significance (as recorded)
- Likely_benign
- Variant type
- missense_variant
- Chromosome / position
- 17:39021137
- HGVS
- NM_000223.4,c.728C>T,p.Thr243Ile
- Allele change
- Missense_T243I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.