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rs2056202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 2 common but increased risk of autism
(T;T) 2 rare decreased risk of autism
Make rs2056202(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position171855970
GeneSLC25A12
is asnp
is mentioned by
dbSNPrs2056202
ebirs2056202
HLIrs2056202
Exacrs2056202
Varsomers2056202
Maprs2056202
PheGenIrs2056202
hapmaprs2056202
1000 genomesrs2056202
hgdprs2056202
ensemblrs2056202
gopubmedrs2056202
geneviewrs2056202
scholarrs2056202
googlers2056202
pharmgkbrs2056202
gwascentralrs2056202
openSNPrs2056202
23andMers2056202
23andMe allrs2056202
SNP Nexus

SNPshotrs2056202
SNPdbers2056202
MSV3drs2056202
GWAS Ctlgrs2056202
GMAF0.2259
Max Magnitude2
? (C;C) (C;T) (T;T) 28
OMIM606053
DescAUTISM, SUSCEPTIBILITY TO, 5; AUTS5
Variant
Relatedalso
OMIM603667
DescSOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER, ARALAR), MEMBER 12;
Variant
Relatedalso


[PMID 19913066] Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan


[PMID 21609426OA-icon.png] A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders


[PMID 15056512] Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.


[PMID 16263864] Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31.


[PMID 17894412] Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism.


[PMID 18348195] An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.


[PMID 19360665] Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism.


[PMID 25921325] Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis