Variant (rsID / SNP)

rs1046428

rs1046428 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSTZ1. Location: chromosome 14, position 77,794,283. The table records no clinical significance for this variant.

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Reference-table entries

GSTZ1Not classified

Variant type: missense_variant
Chromosome / position: 14:77794283
HGVS: NM_001363703.2,c.248T>C,p.Met83Thr
Allele change: Silent

Associated conditions / phenotypes

Bladder Cancer|Breast Cancer

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.