Variant (rsID / SNP)

rs920829

rs920829 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPA1. Location: chromosome 8, position 72,977,703. The table records no clinical significance for this variant.

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Reference-table entries

TRPA1Not classified

Variant type: missense_variant
Chromosome / position: 8:72977703
HGVS: NM_007332.3,c.535G>A,p.Glu179Lys
Allele change: Missense_E179K

Associated conditions / phenotypes

Childhood-Onset Asthma|Asthma|Sickle Cell Disease

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.