Variant (rsID / SNP)
rs4662775
rs4662775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGGT1. Location: chromosome 2, position 128,870,808. The table records no clinical significance for this variant.
Reference-table entries
UGGT1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:128870808
- HGVS
- NM_020120.4,c.672T>C,p.Asn224Asn
- Allele change
- Synonymous_N224N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.