Variant (rsID / SNP)
rs2241759
rs2241759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADCY3. Location: chromosome 2, position 25,064,193. The table records no clinical significance for this variant.
Reference-table entries
ADCY3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:25064193
- HGVS
- NM_001377128.1,c.1131C>T,p.Pro377Pro
- Allele change
- Synonymous_P377P
Associated conditions / phenotypes
Hypertension, Essential
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
