Variant (rsID / SNP)

rs4079366

rs4079366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2A7. Location: chromosome 19, position 41,384,675. The table records no clinical significance for this variant.

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Reference-table entries

CYP2A7Not classified

Variant type: missense_variant
Chromosome / position: 19:41384675
HGVS: NM_000764.3,c.821A>G,p.His274Arg
Allele change: Missense_H274R

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.