Variant (rsID / SNP)
rs13298768
rs13298768 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC16. Location: chromosome 9, position 130,489,743. The table records no clinical significance for this variant.
Reference-table entries
TTC16Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 9:130489743
- HGVS
- NM_144965.3,c.1763A>G,p.Glu588Gly
- Allele change
- Missense_E588G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.