Variant (rsID / SNP)
rs113301777
rs113301777 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNC. Location: chromosome 9, position 117,826,096. The table records no clinical significance for this variant.
Reference-table entries
TNCNot classified
- Variant type
- missense_variant
- Chromosome / position
- 9:117826096
- HGVS
- NM_002160.4,c.3739C>A,p.Leu1247Ile
- Allele change
- Missense_L1247I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.