Variant (rsID / SNP)
rs3897926
rs3897926 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to URAD. Location: chromosome 13, position 28,562,605. The table records no clinical significance for this variant.
Reference-table entries
URADNot classified
- Variant type
- missense_variant
- Chromosome / position
- 13:28562605
- HGVS
- NM_001105577.2,c.170A>C,p.Gln57Pro
- Allele change
- Missense_Q57P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.