Variant (rsID / SNP)
rs2215955
rs2215955 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMPH. Location: chromosome 7, position 38,469,039. The table records no clinical significance for this variant.
Reference-table entries
AMPHNot classified
- Variant type
- intron_variant
- Chromosome / position
- 7:38469039
- HGVS
- NM_001635.4,c.1182+403G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.