Variant (rsID / SNP)
rs3746460
rs3746460 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NECAB3. Location: chromosome 20, position 32,248,163. The table records no clinical significance for this variant.
Reference-table entries
NECAB3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:32248163
- HGVS
- NM_031232.4,c.426G>A,p.Thr142Thr
- Allele change
- Synonymous_T142T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.