Variant (rsID / SNP)
rs2544794
rs2544794 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULT2B1. Location: chromosome 19, position 49,079,246. The table records no clinical significance for this variant.
Reference-table entries
SULT2B1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:49079246
- HGVS
- NM_177973.2,c.120C>T,p.Pro40Pro
- Allele change
- Synonymous_P40P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
