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Variant (rsID / SNP)

rs113164681

CYP2C19

rs113164681 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C19. Location: chromosome 10, position 96,520,433. 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
10:96520433
Cytoband
10q23.33
HGVS
NC_000010.11:g.94760676C>T

Public references

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