Variant (rsID / SNP)
rs3787430
rs3787430 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HRH3. Location: chromosome 20, position 60,791,422. The table records no clinical significance for this variant.
Reference-table entries
HRH3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:60791422
- HGVS
- NM_007232.3,c.978G>A,p.Pro326Pro
- Allele change
- Synonymous_P326P
Associated conditions / phenotypes
Narcolepsy|Cocaine Dependence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.