Variant (rsID / SNP)
rs14065
rs14065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM218. Location: chromosome 11, position 124,972,208. The table records no clinical significance for this variant.
Reference-table entries
TMEM218Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:124972208
- HGVS
- NM_001387255.1,c.35T>C,p.Leu12Ser
- Allele change
- Silent
Associated conditions / phenotypes
Silent|Missense_L12S|Silent|Missense_L12S|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.