Variant (rsID / SNP)
rs3737353
rs3737353 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to L3MBTL4. Location: chromosome 18, position 5,956,238. The table records no clinical significance for this variant.
Reference-table entries
L3MBTL4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:5956238
- HGVS
- NM_001365770.2,c.1853G>A,p.Gly618Asp
- Allele change
- Missense_G609D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.