Variant (rsID / SNP)
rs2904979
rs2904979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A20P. Location: chromosome 11, position 65,000,719. The table records no clinical significance for this variant.
Reference-table entries
SLC22A20PNot classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 11:65000719
- HGVS
- NR_033396.1,n.1180C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.