Variant (rsID / SNP)

rs2071426

rs2071426 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C8. Location: chromosome 10, position 96,828,323. 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: 10:96828323
Cytoband: 10q23.33
HGVS: NM_000770.3(CYP2C8):c.168+669A>G
Allele change: Silent

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.