Variant (rsID / SNP)

rs55633891

rs55633891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRNA9. Location: chromosome 4, position 40,356,041. The table records no clinical significance for this variant.

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Reference-table entries

CHRNA9Not classified

Variant type: missense_variant
Chromosome / position: 4:40356041
HGVS: NM_017581.4,c.944C>T,p.Ala315Val
Allele change: Missense_A315V

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.