Variant (rsID / SNP)

rs1051730

rs1051730 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRNA3. Location: chromosome 15, position 78,894,339. Clinical significance in the table: risk factor.

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Reference-table entries

CHRNA3Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 15:78894339
Cytoband: 15q25.1
HGVS: NM_000743.5(CHRNA3):c.645C>T (p.Tyr215=)
Allele change: Silent

Associated conditions / phenotypes

Lung cancer susceptibility 2|Smoking as a quantitative trait locus 3

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.