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Variant (rsID / SNP)

rs2056900

CYP4A22

rs2056900 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4A22. Location: chromosome 1, position 47,607,785. The table records no clinical significance for this variant.

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Reference-table entries

CYP4A22Not classified
Variant type
missense_variant
Chromosome / position
1:47607785
HGVS
NM_001010969.4,c.388G>A,p.Gly130Ser
Allele change
Missense_G130S

Public references

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