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rs17638629

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17638629(G;G)
Make rs17638629(G;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12114557
GeneZNF788
is asnp
is mentioned by
dbSNPrs17638629
ebirs17638629
HLIrs17638629
Exacrs17638629
Varsomers17638629
Maprs17638629
PheGenIrs17638629
hapmaprs17638629
1000 genomesrs17638629
hgdprs17638629
ensemblrs17638629
gopubmedrs17638629
geneviewrs17638629
scholarrs17638629
googlers17638629
pharmgkbrs17638629
gwascentralrs17638629
openSNPrs17638629
23andMers17638629
23andMe allrs17638629
SNP Nexus

SNPshotrs17638629
SNPdbers17638629
MSV3drs17638629
GWAS Ctlgrs17638629
GMAF0.03489
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 7 x 10^-6) for Trails A performance
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000007
Odds Ratio None None