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rs16946931

From SNPedia

Orientationplus
Stabilizedplus
Make rs16946931(C;C)
Make rs16946931(C;T)
Make rs16946931(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position49108595
is asnp
is mentioned by
dbSNPrs16946931
ebirs16946931
HLIrs16946931
Exacrs16946931
Varsomers16946931
Maprs16946931
PheGenIrs16946931
hapmaprs16946931
1000 genomesrs16946931
hgdprs16946931
ensemblrs16946931
gopubmedrs16946931
geneviewrs16946931
scholarrs16946931
googlers16946931
pharmgkbrs16946931
gwascentralrs16946931
openSNPrs16946931
23andMers16946931
23andMe allrs16946931
SNP Nexus

SNPshotrs16946931
SNPdbers16946931
MSV3drs16946931
GWAS Ctlgrs16946931
GMAF0.2782
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24133439OA-icon.png] Genome-wide association study of autistic-like traits in a general population study of young adults