Variant (rsID / SNP)

rs7819749

rs7819749 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPA1. Location: chromosome 8, position 72,975,801. The table records no clinical significance for this variant.

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Reference-table entries

TRPA1Not classified

Variant type: missense_variant
Chromosome / position: 8:72975801
HGVS: NM_007332.3,c.558A>C,p.Lys186Asn
Allele change: Missense_K186N

Associated conditions / phenotypes

Pulmonary Disease, Chronic Obstructive

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.