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rs9616915

From SNPedia

Orientationplus
Stabilizedplus
Make rs9616915(C;C)
Make rs9616915(C;T)
Make rs9616915(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position50679152
GeneSHANK3
is asnp
is mentioned by
dbSNPrs9616915
ebirs9616915
HLIrs9616915
Exacrs9616915
Varsomers9616915
Maprs9616915
PheGenIrs9616915
hapmaprs9616915
1000 genomesrs9616915
hgdprs9616915
ensemblrs9616915
gopubmedrs9616915
geneviewrs9616915
scholarrs9616915
googlers9616915
pharmgkbrs9616915
gwascentralrs9616915
openSNPrs9616915
23andMers9616915
23andMe allrs9616915
SNP Nexus

SNPshotrs9616915
SNPdbers9616915
MSV3drs9616915
GWAS Ctlgrs9616915
GMAF0.3581
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24398551] A commonly carried genetic variant, rs9616915, in SHANK3 gene is associated with a reduced risk of autism spectrum disorder: replication in a Chinese population


[PMID 19384346OA-icon.png] Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.


[PMID 19566951OA-icon.png] Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.


[PMID 27271042] The association of SHANK3 gene polymorphism and autism.