Variant (rsID / SNP)
rs2280134
rs2280134 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ART1. Location: chromosome 11, position 3,681,519. The table records no clinical significance for this variant.
Reference-table entries
ART1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:3681519
- HGVS
- NM_004314.3,c.770T>C,p.Leu257Pro
- Allele change
- Missense_L257P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
