Variant (rsID / SNP)
rs911159
rs911159 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CASS4. Location: chromosome 20, position 55,012,318. The table records no clinical significance for this variant.
Reference-table entries
CASS4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:55012318
- HGVS
- NM_001164116.2,c.135G>A,p.Val45Val
- Allele change
- Synonymous_V45V
Associated conditions / phenotypes
Alzheimer Disease|Aging
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.