Variant (rsID / SNP)
rs12878
rs12878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMTOR4. Location: chromosome 7, position 99,747,130. The table records no clinical significance for this variant.
Reference-table entries
LAMTOR4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:99747130
- HGVS
- NM_001394587.1,c.90G>A,p.Ala30Ala
- Allele change
- Silent
Associated conditions / phenotypes
Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.