Variant (rsID / SNP)

rs915909

rs915909 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2E1. Location: chromosome 10, position 135,347,397. Clinical significance in the table: Benign.

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Reference-table entries

CYP2E1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:135347397
Cytoband: 10q26.3
HGVS: NM_000773.4(CYP2E1):c.963= (p.Ile321=)
Allele change: Synonymous_I321I

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.