Variant (rsID / SNP)
rs973126
rs973126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAPSS1. Location: chromosome 4, position 108,641,300. The table records no clinical significance for this variant.
Reference-table entries
PAPSS1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:108641300
- HGVS
- NM_005443.5,c.36A>G,p.Lys12Lys
- Allele change
- Synonymous_K12K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.