Variant (rsID / SNP)
rs7593557
rs7593557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM8. Location: chromosome 2, position 234,863,788. The table records no clinical significance for this variant.
Reference-table entries
TRPM8Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:234863788
- HGVS
- NM_024080.5,c.1256G>A,p.Ser419Asn
- Allele change
- Missense_S419N
Associated conditions / phenotypes
Asthma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.