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rs17070284

From SNPedia

Orientationplus
Stabilizedplus
Make rs17070284(C;C)
Make rs17070284(C;T)
Make rs17070284(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position78785289
is asnp
is mentioned by
dbSNPrs17070284
ebirs17070284
HLIrs17070284
Exacrs17070284
Varsomers17070284
Maprs17070284
PheGenIrs17070284
hapmaprs17070284
1000 genomesrs17070284
hgdprs17070284
ensemblrs17070284
gopubmedrs17070284
geneviewrs17070284
scholarrs17070284
googlers17070284
pharmgkbrs17070284
gwascentralrs17070284
openSNPrs17070284
23andMers17070284
23andMe allrs17070284
SNP Nexus

SNPshotrs17070284
SNPdbers17070284
MSV3drs17070284
GWAS Ctlgrs17070284
GMAF0.1295
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 3 x 10^-6) for Controlled Oral Word Association (COWA) test 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 0.000003
Odds Ratio None None