Variant (rsID / SNP)
rs4888444
rs4888444 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TERF2IP. Location: chromosome 16, position 75,690,279. The table records no clinical significance for this variant.
Reference-table entries
TERF2IPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 16:75690279
- HGVS
- NM_018975.4,c.970A>G,p.Lys324Glu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.