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rs7766973

From SNPedia

Orientationplus
Stabilizedplus
Make rs7766973(C;C)
Make rs7766973(C;T)
Make rs7766973(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position15267820
GeneJARID2
is asnp
is mentioned by
dbSNPrs7766973
ebirs7766973
HLIrs7766973
Exacrs7766973
Varsomers7766973
Maprs7766973
PheGenIrs7766973
hapmaprs7766973
1000 genomesrs7766973
hgdprs7766973
ensemblrs7766973
gopubmedrs7766973
geneviewrs7766973
scholarrs7766973
googlers7766973
pharmgkbrs7766973
gwascentralrs7766973
openSNPrs7766973
23andMers7766973
23andMe allrs7766973
SNP Nexus

SNPshotrs7766973
SNPdbers7766973
MSV3drs7766973
GWAS Ctlgrs7766973
GMAF0.4582
Max Magnitude
? (C;C) (C;T) (T;T) 28
rs7766973 is a SNP in the jumonji, AT rich interactive domain 2 JARID2 gene.

Significantly (p = 2 x 10e-7) but weakly associated with autism based on a GWAS study of 1,000+ affected families. However, upon attempted replication, rs7766973 did not meet genome-wide significance.[PMID 19812673OA-icon.png]

Nonetheless, a French company (Integragen) announced in 2011 ([1] that is was licensing the use of this SNP for identifying children at increased risk for autism, perhaps by combining rs7766973 with other autism-related SNPs.