Variant (rsID / SNP)
rs352493
rs352493 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIRT6. Location: chromosome 19, position 4,180,836. The table records no clinical significance for this variant.
Reference-table entries
SIRT6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:4180836
- HGVS
- NM_016539.4,c.137G>A,p.Ser46Asn
- Allele change
- Silent
Associated conditions / phenotypes
Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Missense_S46N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.