Variant (rsID / SNP)

rs10009228

rs10009228 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRNA9. Location: chromosome 4, position 40,356,422. The table records no clinical significance for this variant.

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Reference-table entries

CHRNA9Not classified

Variant type: missense_variant
Chromosome / position: 4:40356422
HGVS: NM_017581.4,c.1325A>G,p.Asn442Ser
Allele change: Missense_N442S

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.