Variant (rsID / SNP)

rs1138272

rs1138272 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSTP1. Location: chromosome 11, position 67,353,579. Clinical significance in the table: Benign.

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Reference-table entries

GSTP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:67353579
Cytoband: 11q13.2
HGVS: NM_000852.4(GSTP1):c.341C>T (p.Ala114Val)
Allele change: Missense_A197V

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.