Variant (rsID / SNP)
rs56295968
rs56295968 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM218. Location: chromosome 11, position 124,972,553. The table records no clinical significance for this variant.
Reference-table entries
TMEM218Not classified
- Variant type
- stop_gained
- Chromosome / position
- 11:124972553
- HGVS
- NM_001387250.1,c.9G>A,p.Trp3*
- Allele change
- Silent
Associated conditions / phenotypes
Silent|Nonsense_W3X|Silent|Nonsense_W3X|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.