Variant (rsID / SNP)
rs3730477
rs3730477 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLL. Location: chromosome 10, position 103,340,056. The table records no clinical significance for this variant.
Reference-table entries
POLLNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:103340056
- HGVS
- NM_001174084.2,c.1312C>T,p.Arg438Trp
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.