Variant (rsID / SNP)

rs2405599

rs2405599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4A22. Location: chromosome 1, position 47,611,598. The table records no clinical significance for this variant.

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Reference-table entries

CYP4A22Not classified

Variant type: missense_variant
Chromosome / position: 1:47611598
HGVS: NM_001010969.4,c.1283T>C,p.Leu428Pro
Allele change: Missense_L428P

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.