Variant (rsID / SNP)
rs9890913
rs9890913 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASIC2. Location: chromosome 17, position 31,618,551. The table records no clinical significance for this variant.
Reference-table entries
ASIC2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:31618551
- HGVS
- NM_183377.2,c.583C>T,p.Leu195Leu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.