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rs9257616

From SNPedia

Orientationplus
Stabilizedplus
Make rs9257616(A;A)
Make rs9257616(A;G)
Make rs9257616(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position29212944
is asnp
is mentioned by
dbSNPrs9257616
ebirs9257616
HLIrs9257616
Exacrs9257616
Varsomers9257616
Maprs9257616
PheGenIrs9257616
hapmaprs9257616
1000 genomesrs9257616
hgdprs9257616
ensemblrs9257616
gopubmedrs9257616
geneviewrs9257616
scholarrs9257616
googlers9257616
pharmgkbrs9257616
gwascentralrs9257616
openSNPrs9257616
23andMers9257616
23andMe allrs9257616
SNP Nexus

SNPshotrs9257616
SNPdbers9257616
MSV3drs9257616
GWAS Ctlgrs9257616
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24047820OA-icon.png]
Trait Social communication problems
Title Common variation contributes to the genetic architecture of social communication traits.
Risk Allele G
P-val 3E-7
Odds Ratio .09 [0.058-0.128] unit increase