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rs7834018

From SNPedia

Orientationplus
Stabilizedplus
Make rs7834018(C;C)
Make rs7834018(C;T)
Make rs7834018(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position71649507
is asnp
is mentioned by
dbSNPrs7834018
ebirs7834018
HLIrs7834018
Exacrs7834018
Varsomers7834018
Maprs7834018
PheGenIrs7834018
hapmaprs7834018
1000 genomesrs7834018
hgdprs7834018
ensemblrs7834018
gopubmedrs7834018
geneviewrs7834018
scholarrs7834018
googlers7834018
pharmgkbrs7834018
gwascentralrs7834018
openSNPrs7834018
23andMers7834018
23andMe allrs7834018
SNP Nexus

SNPshotrs7834018
SNPdbers7834018
MSV3drs7834018
GWAS Ctlgrs7834018
GMAF0.2557
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22843504OA-icon.png]
Trait Autism
Title Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
Risk Allele
P-val 8E-7
Odds Ratio 1.56 [1.3-1.89]