Variant (rsID / SNP)
rs3132679
rs3132679 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM31. Location: chromosome 6, position 30,075,843. The table records no clinical significance for this variant.
Reference-table entries
TRIM31Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30075843
- HGVS
- NM_007028.5,c.870A>G,p.Leu290Leu
- Allele change
- Synonymous_L290L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.