Variant (rsID / SNP)
rs6795271
rs6795271 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUP210. Location: chromosome 3, position 13,399,786. The table records no clinical significance for this variant.
Reference-table entries
NUP210Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:13399786
- HGVS
- NM_024923.4,c.2264C>T,p.Ala755Val
- Allele change
- Missense_A755V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.