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rs6716901

From SNPedia

Orientationplus
Stabilizedplus
Make rs6716901(A;A)
Make rs6716901(A;G)
Make rs6716901(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position171816943
GeneSLC25A12
is asnp
is mentioned by
dbSNPrs6716901
dbSNP (old)rs6716901
ClinGenrs6716901
ebirs6716901
HLIrs6716901
Exacrs6716901
Gnomadrs6716901
Varsomers6716901
Maprs6716901
PheGenIrs6716901
Biobankrs6716901
1000 genomesrs6716901
hgdprs6716901
ensemblrs6716901
gopubmedrs6716901
geneviewrs6716901
scholarrs6716901
googlers6716901
pharmgkbrs6716901
gwascentralrs6716901
openSNPrs6716901
23andMers6716901
23andMe allrs6716901
SNP Nexus

SNPshotrs6716901
SNPdbers6716901
MSV3drs6716901
GWAS Ctlgrs6716901
Max Magnitude
? (A;A) (A;G) (G;G) 28
In a study size of 117 Caucasians with Asperger syndrome and 426 controls "Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome" [PMID 24679184OA-icon.png] found association of this SNP's minor allele (A) in SLC25A12 gene with Asperger syndrome. Minor allele (A) was associated with OR 1.70 (0.98-3.02) P=0.008 after correcting for multiple testing. The study did not replicate previously reported associations with rs2056202 and rs3765166 which authors speculate could be due to differences in diagnosing AS and heterogenity of sample, though they admit to limitation of sample size and lack of replication sample.