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Variant (rsID / SNP)

rs12564525

CYP4A22

rs12564525 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4A22. Location: chromosome 1, position 47,607,281. The table records no clinical significance for this variant.

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Reference-table entries

CYP4A22Not classified
Variant type
missense_variant
Chromosome / position
1:47607281
HGVS
NM_001010969.4,c.376C>T,p.Arg126Trp
Allele change
Missense_R126W

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.