Variant (rsID / SNP)
rs10879901
rs10879901 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPS2. Location: chromosome 12, position 75,715,330. The table records no clinical significance for this variant.
Reference-table entries
CAPS2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:75715330
- HGVS
- NM_001355023.4,c.318G>T,p.Leu106Phe
- Allele change
- Silent
Associated conditions / phenotypes
Missense_L39F|Silent|Missense_L75F|Missense_L75F|Silent|Silent|Missense_L39F|Silent|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.