Variant (rsID / SNP)
rs6554354
rs6554354 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AASDH. Location: chromosome 4, position 57,237,683. The table records no clinical significance for this variant.
Reference-table entries
AASDHNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:57237683
- HGVS
- NM_001323890.2,c.795C>T,p.Ser265Ser
- Allele change
- Synonymous_S112S
Associated conditions / phenotypes
Silent|Synonymous_S265S|Synonymous_S112S|Synonymous_S265S|Synonymous_S265S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.