Variant (rsID / SNP)

rs2515641

rs2515641 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2E1. Location: chromosome 10, position 135,351,362. 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: 10:135351362
Cytoband: 10q26.3
HGVS: NM_000773.4(CYP2E1):c.1263= (p.Phe421=)
Allele change: Synonymous_F421F

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.