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rs4775031

From SNPedia

Orientationplus
Stabilizedplus
Make rs4775031(A;A)
Make rs4775031(A;C)
Make rs4775031(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position58343384
GeneLOC101928635
is asnp
is mentioned by
dbSNPrs4775031
dbSNP (classic)rs4775031
ClinGenrs4775031
ebirs4775031
HLIrs4775031
Exacrs4775031
Gnomadrs4775031
Varsomers4775031
LitVarrs4775031
Maprs4775031
PheGenIrs4775031
Biobankrs4775031
1000 genomesrs4775031
hgdprs4775031
ensemblrs4775031
geneviewrs4775031
scholarrs4775031
googlers4775031
pharmgkbrs4775031
gwascentralrs4775031
openSNPrs4775031
23andMers4775031
SNPshotrs4775031
SNPdbers4775031
MSV3drs4775031
GWAS Ctlgrs4775031
GMAF0.1676
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 2 x 10^-6) for Trails B 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 0.000002
Odds Ratio None None