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rs7792596

From SNPedia

Orientationplus
Stabilizedplus
Make rs7792596(C;C)
Make rs7792596(C;T)
Make rs7792596(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position94380322
GeneLOC101927525
is asnp
is mentioned by
dbSNPrs7792596
ebirs7792596
HLIrs7792596
Exacrs7792596
Varsomers7792596
Maprs7792596
PheGenIrs7792596
hapmaprs7792596
1000 genomesrs7792596
hgdprs7792596
ensemblrs7792596
gopubmedrs7792596
geneviewrs7792596
scholarrs7792596
googlers7792596
pharmgkbrs7792596
gwascentralrs7792596
openSNPrs7792596
23andMers7792596
23andMe allrs7792596
SNP Nexus

SNPshotrs7792596
SNPdbers7792596
MSV3drs7792596
GWAS Ctlgrs7792596
GMAF0.388
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22449649]
Trait
Title Genome-wide association study of intelligence: additive effects of novel brain expressed genes.
Risk Allele
P-val 6E-7
Odds Ratio 4.1300 None