Variant (rsID / SNP)
rs2251761
rs2251761 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CADPS2. Location: chromosome 7, position 122,303,321. The table records no clinical significance for this variant.
Reference-table entries
CADPS2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:122303321
- HGVS
- NM_001363389.2,c.756G>A,p.Leu252Leu
- Allele change
- Synonymous_L252L
Associated conditions / phenotypes
Synonymous_L252L|Synonymous_L252L|Synonymous_L252L|Synonymous_L252L|Synonymous_L252L|Synonymous_L252L|Synonymous_L252L|Synonymous_L252L|Synonymous_L91L|Synonymous_L252L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.