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rs1891498

From SNPedia

Orientationminus
Stabilizedminus
Make rs1891498(C;C)
Make rs1891498(C;T)
Make rs1891498(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position147754660
GeneLOC102723321
is asnp
is mentioned by
dbSNPrs1891498
ebirs1891498
HLIrs1891498
Exacrs1891498
Varsomers1891498
Maprs1891498
PheGenIrs1891498
hapmaprs1891498
1000 genomesrs1891498
hgdprs1891498
ensemblrs1891498
gopubmedrs1891498
geneviewrs1891498
scholarrs1891498
googlers1891498
pharmgkbrs1891498
gwascentralrs1891498
openSNPrs1891498
23andMers1891498
23andMe allrs1891498
SNP Nexus

SNPshotrs1891498
SNPdbers1891498
MSV3drs1891498
GWAS Ctlgrs1891498
GMAF0.1309
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive performance
Title Common genetic variation and performance on standardized cognitive tests.
Risk Allele
P-val 9E-6
Odds Ratio NR NR