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Variant (rsID / SNP)

rs111490789

CYP2C19

rs111490789 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C19. Location: chromosome 10, position 96,520,443. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

CYP2C19Other
Clinical significance (as recorded)
no interpretation for the single variant
Variant type
single nucleotide variant
Chromosome / position
10:96520443
Cytoband
10q23.33
HGVS
NM_000769.4(CYP2C19):c.-2020C>A

Public references

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