rs2292813

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	normal
(C;T)	2	decreased risk of autism
(T;T)	2	decreased risk of autism

Reference

GRCh38 38.1/141

Chromosome

2

Position

171787719

Gene

SLC25A12

is a	snp
is	mentioned by
dbSNP	rs2292813
dbSNP (classic)	rs2292813
ClinGen	rs2292813
ebi	rs2292813
HLI	rs2292813
Exac	rs2292813
Gnomad	rs2292813
Varsome	rs2292813
LitVar	rs2292813
Map	rs2292813
PheGenI	rs2292813
Biobank	rs2292813
1000 genomes	rs2292813
hgdp	rs2292813
ensembl	rs2292813
geneview	rs2292813
scholar	rs2292813
google	rs2292813
pharmgkb	rs2292813
gwascentral	rs2292813
openSNP	rs2292813
23andMe	rs2292813
SNPshot	rs2292813
SNPdbe	rs2292813
MSV3d	rs2292813
GWAS Ctlg	rs2292813

GMAF

0.18

Max Magnitude

2

?	(C;C) (C;T) (T;T)	28

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

[PMID 21609426] 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 19360665] Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism.

[PMID 20678243] Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.

[PMID 22739633] The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families

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