Variant (rsID / SNP)
rs1827293
rs1827293 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NBPF3. Location: chromosome 1, position 21,795,388. The table records no clinical significance for this variant.
Reference-table entries
NBPF3Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 1:21795388
- HGVS
- NM_032264.6,c.341A>G,p.Tyr114Cys
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.