Variant (rsID / SNP)
rs2305271
rs2305271 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NTM. Location: chromosome 11, position 132,177,633. The table records no clinical significance for this variant.
Reference-table entries
NTMNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:132177633
- HGVS
- NM_001352001.2,c.577A>C,p.Arg193Arg
- Allele change
- Synonymous_R193R
Associated conditions / phenotypes
Synonymous_R193R|Silent|Synonymous_R152R|Silent|Synonymous_R193R|Silent|Silent|Synonymous_R193R|Synonymous_R174R|Silent|Synonymous_R193R|Synonymous_R193R|Synonymous_R193R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.