Variant (rsID / SNP)
rs542234
rs542234 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC9A8. Location: chromosome 20, position 48,491,258. The table records no clinical significance for this variant.
Reference-table entries
SLC9A8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:48491258
- HGVS
- NM_001260491.2,c.1023T>G,p.Leu341Leu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.