Variant (rsID / SNP)

rs56258513

rs56258513 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4A22. Location: chromosome 1, position 47,606,470. The table records no clinical significance for this variant.

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Reference-table entries

CYP4A22Not classified

Variant type: missense_variant
Chromosome / position: 1:47606470
HGVS: NM_001010969.4,c.214C>A,p.Leu72Ile
Allele change: Missense_L72I

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.