Variant (rsID / SNP)

rs118203757

rs118203757 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C19. Location: chromosome 10, position 96,602,636. 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: 10:96602636
Cytoband: 10q23.33
HGVS: NM_000769.4(CYP2C19):c.1004G>A (p.Arg335Gln)
Allele change: Missense_R335Q

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.