Table 1 GST allelic variants associated with cancer risk and other diseases
Gene | Allelic variant | Modification | OMIM number | Diseases | Ref. |
|---|---|---|---|---|---|
GSTM1 | GSTM1*O | Gene deletion | 138350 | Uterine leiomyoma, hypertension, oral leukoplakia, prostate cancer, chronic myeloid leukemia, breast cancer, epilepsy | |
GSTT1 | GSTT1*O | Gene deletion | 600436 | Uterine leiomyoma, hypertension, oral leukoplakia, brain tumour, breast cancer, coronary heart disease, psoriasisa, epilepsy | |
GSTP1 | GSTP1*B | Ile105Val | 134660.0002 | chronic myeloid leukemia, Parkinson’s disease, Amyotrophic lateral sclerosis | |
GSTP1*C | Ile105Val/Ala114Val | 134660.0003 | Alzheimer’s disease, Parkinson’s disease | ||
GSTP1*D | Ala114Val | — | Brain tumour, Parkinson’s disease | ||
GSTA1 | GSTA1*B | -69(C/T), mutation promoter | 138359 | Psoriasisb | |
GSTO1 | GSTO1*B | Glu155 deletion | 605482 | Alzheimer’s disease | |
GSTO2 | GSTO2*B c | Asn142Asp | 612314 | Breast cancer | |
GSTO2*C c | Ala183Gly | — | Spinocerebellar ataxia type 2 |