Variant (rsID / SNP)

rs16969968

rs16969968 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRNA5. Location: chromosome 15, position 78,882,925. Clinical significance in the table: drug response.

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Reference-table entries

CHRNA5Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 15:78882925
Cytoband: 15q25.1
HGVS: NM_000745.4(CHRNA5):c.1192G>A (p.Asp398Asn)
Allele change: Silent

Associated conditions / phenotypes

Lung cancer susceptibility 2|Smoking as a quantitative trait locus 3|nicotine response - Toxicity

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.