Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768623239
rs768623239
Entrez Id: 2944;2946
Gene Symbol: GSTM1;GSTM2
GSTM1;GSTM2
CUI: C0029456
Disease:
Osteoporosis
0.010 GeneticVariation BEFREE The GSTT1 deletion was associated with a higher frequency of the NMPA to homozygous deletion (p = 0.008), GSTP1 + 313A > G with a minor risk of osteoporosis (p = 0.036), and patient age ≤ 154 months (p = 0.044) with the AA genotype. 24593045 2014