EVAapplication/xmlftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB101865/casos_MTHFR_ASD_EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB101865/casos_MTHFR_ASD_EVA.vcf.gz.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB101865/controles_MTHFR_ASD_EVA.vcf.gz.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB101865/controles_MTHFR_ASD_EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB101865/controles_MTHFR_ASD_EVA.vcf.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB101865/casos_MTHFR_ASD_EVA.vcf.csiprimaryOK200Genotyping By ArrayGenomicsEBI-Homo Sapienshttps://www.ebi.ac.uk/eva/?eva-study=PRJEB101865EVAfalseMTHFR C677T is not associated with autism spectrum disorder in a Mexican cohortWe performed an association study to see if the SNV variant MTHFR C677T is associated with individuals with autism spectrum disorder in a Mexican cohort2025-11-01PRJEB1018659606