Variant (rsID / SNP)
rs16986718
rs16986718 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP4. Location: chromosome 19, position 56,369,314. The table records no clinical significance for this variant.
Reference-table entries
NLRP4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:56369314
- HGVS
- NM_134444.5,c.555G>A,p.Thr185Thr
- Allele change
- Synonymous_T185T
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.