Variant (rsID / SNP)
rs34350265
rs34350265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL27A1. Location: chromosome 9, position 116,973,273. The table records no clinical significance for this variant.
Reference-table entries
COL27A1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:116973273
- HGVS
- NM_032888.4,c.2334C>T,p.Gly778Gly
- Allele change
- Synonymous_G778G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.