Variant (rsID / SNP)

rs1058930

rs1058930 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C8. Location: chromosome 10, position 96,818,119. Clinical significance in the table: Benign.

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Reference-table entries

CYP2C8Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:96818119
Cytoband: 10q23.33
HGVS: CYP2C8*4
Allele change: Missense_I194M

Associated conditions / phenotypes

CYP2C8 POLYMORPHISM

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.