Variant (rsID / SNP)
rs2076425
rs2076425 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMF1. Location: chromosome 16, position 929,711. The table records no clinical significance for this variant.
Reference-table entries
LMF1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 16:929711
- HGVS
- NM_022773.4,c.756G>A,p.Ala252Ala
- Allele change
- Silent
Associated conditions / phenotypes
Synonymous_A119A|Synonymous_A35A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.