Variant (rsID / SNP)
rs79719081
rs79719081 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VIM. Location: chromosome 10, position 17,277,158. Clinical significance in the table: Benign.
Reference-table entries
VIMBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:17277158
- Cytoband
- 10p13
- HGVS
- NM_003380.5(VIM):c.1009-10C>T
- Allele change
- Silent
Associated conditions / phenotypes
Cataract 30
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.