Variant (rsID / SNP)
rs229519
rs229519 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C1QTNF6. Location: chromosome 22, position 37,578,579. The table records no clinical significance for this variant.
Reference-table entries
C1QTNF6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 22:37578579
- HGVS
- NM_031910.4,c.486G>A,p.Thr162Thr
- Allele change
- Synonymous_T162T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.