rs2292813, SLC25A12

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.040 GeneticVariation BEFREE In addition, the G-C haplotype of rs1023159-rs1051266 in SCL19A1 (OR = 0.71, 95% CI = 0.51-0.98, P = 0.0389) and C-C haplotype of rs2056202-rs2292813 in SLC25A12 (OR = 0.58, 95% CI = 0.35-0.96, P = 0.0325) were associated with decreased risks of childhood ASD. 28536923 2017
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.040 GeneticVariation BEFREE We found a statistically significant association between ASD and variant in rs2292813 (OR = 1.190, 95% CI 1.052-1.346, P = 0.006) as well as in rs2056202 (OR = 1.206, 95% CI 1.035-1.405, P = 0.016). 25663199 2016
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.040 GeneticVariation BEFREE Our meta-analysis suggests that rs2056202 and rs2292813</span> in </span>SLC25A12 may contribute significantly to ASD risk. 25921325 2015
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.040 GeneticVariation BEFREE We genotyped two single nucleotide polymorphisms (SNPs, rs2056202 and rs2292813) of the SLC25A12 gene that were previously reported to be associated with autism in 465 patients (402 males and 63 females) and 450 control subjects (227 males and 223 females) from Taiwan. 19913066 2010
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.040 GeneticVariation BEFREE Family-based association analysis of two SNPs, rs2056202 and rs2292813, previously shown to be associated with autism was performed in two samples with different phenotypic characteristics. 19360665 2008
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.040 GeneticVariation BEFREE Evidence for a genetic association between autism and two single nucleotide polymorphisms (SNPs), rs2056202 and rs2292813, in the mitochondrial aspartate/glutamate carrier (SLC25A12) gene led us to ask whether any of the four previously identified familial traits in autism spectrum disorders (ASD) varied by these SNPs. 17894412 2008
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.040 GeneticVariation BEFREE Evidence for a genetic association between autism and two single nucleotide polymorphisms (SNPs), rs2056202 and rs2292813, in the mitochondrial aspartate/glutamate carrier (SLC25A12) gene led us to ask whether any of the four previously identified familial traits in autism spectrum disorders (ASD) varied by these SNPs. 17894412 2008
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.040 GeneticVariation BEFREE In agreement with the recent study, the authors found significant association between autism and the C alleles of both rs2056202 and rs2292813 as well as the two-marker haplotype. 16263864 2005
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
0.010 GeneticVariation BEFREE Evidence for a genetic association between autism and two single nucleotide polymorphisms (SNPs), rs2056202 and rs2292813, in the mitochondrial aspartate/glutamate carrier (SLC25A12) gene led us to ask whether any of the four previously identified familial traits in autism spectrum disorders (ASD) varied by these SNPs. 17894412 2008