The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

We analyzed the allelic and genotypic frequencies of the glutathione-S-transferase P1 (GSTPI) rs1695 single nucleotide polymorphism (SNP) in 290 patients with multiple sclerosis (MS) and in 310 healthy controls. We found no significant association between the rs1695 variant and MS. Among MS patients...

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Published inCellular & molecular immunology Vol. 12; no. 6; pp. 777 - 779
Main Authors Agúndez, José A G, García-Martín, Elena, Martínez, Carmen, Benito-León, Julián, Millán-Pascual, Jorge, Díaz-Sánchez, María, Calleja, Patricia, Pisa, Diana, Turpín-Fenoll, Laura, Alonso-Navarro, Hortensia, Ayuso-Peralta, Lucía, Torrecillas, Dolores, García-Albea, Esteban, Plaza-Nieto, José Francisco, Jiménez-Jiménez, Félix Javier
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.11.2015
Nature Publishing Group
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Summary:We analyzed the allelic and genotypic frequencies of the glutathione-S-transferase P1 (GSTPI) rs1695 single nucleotide polymorphism (SNP) in 290 patients with multiple sclerosis (MS) and in 310 healthy controls. We found no significant association between the rs1695 variant and MS. Among MS patients, there was no relationship between the rs1695 variant and either gender, clinical type of MS or the age of onset of MS.
Bibliography:11-4987/R
We analyzed the allelic and genotypic frequencies of the glutathione-S-transferase P1 (GSTPI) rs1695 single nucleotide polymorphism (SNP) in 290 patients with multiple sclerosis (MS) and in 310 healthy controls. We found no significant association between the rs1695 variant and MS. Among MS patients, there was no relationship between the rs1695 variant and either gender, clinical type of MS or the age of onset of MS.
ObjectType-Article-1
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ISSN:1672-7681
2042-0226
DOI:10.1038/cmi.2014.121