Variant (rsID / SNP)
rs3735124
rs3735124 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CARD11. Location: chromosome 7, position 2,957,005. The table records no clinical significance for this variant.
Reference-table entries
CARD11Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:2957005
- HGVS
- NM_001324281.3,c.2622A>G,p.Pro874Pro
- Allele change
- Synonymous_P874P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.