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rs9942541

From SNPedia

Orientationplus
Stabilizedplus
Make rs9942541(C;C)
Make rs9942541(C;T)
Make rs9942541(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position39156906
is asnp
is mentioned by
dbSNPrs9942541
ebirs9942541
HLIrs9942541
Exacrs9942541
Varsomers9942541
Maprs9942541
PheGenIrs9942541
hapmaprs9942541
1000 genomesrs9942541
hgdprs9942541
ensemblrs9942541
gopubmedrs9942541
geneviewrs9942541
scholarrs9942541
googlers9942541
pharmgkbrs9942541
gwascentralrs9942541
openSNPrs9942541
23andMers9942541
23andMe allrs9942541
SNP Nexus

SNPshotrs9942541
SNPdbers9942541
MSV3drs9942541
GWAS Ctlgrs9942541
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24564958OA-icon.png]
Trait Social communication problems
Title Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.
Risk Allele T
P-val 5E-6
Odds Ratio .23 [0.13-0.33] unit increase