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rs10475598

From SNPedia

Orientationplus
Stabilizedplus
Make rs10475598(C;C)
Make rs10475598(C;T)
Make rs10475598(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position174221435
is asnp
is mentioned by
dbSNPrs10475598
ebirs10475598
HLIrs10475598
Exacrs10475598
Varsomers10475598
Maprs10475598
PheGenIrs10475598
hapmaprs10475598
1000 genomesrs10475598
hgdprs10475598
ensemblrs10475598
gopubmedrs10475598
geneviewrs10475598
scholarrs10475598
googlers10475598
pharmgkbrs10475598
gwascentralrs10475598
openSNPrs10475598
23andMers10475598
23andMe allrs10475598
SNP Nexus

SNPshotrs10475598
SNPdbers10475598
MSV3drs10475598
GWAS Ctlgrs10475598
GMAF0.4385
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21130836OA-icon.png]
Trait
Title Whole genome association scan for genetic polymorphisms influencing information processing speed
Risk Allele T
P-val 8E-7
Odds Ratio 0.1500 [0.09-0.21] unit increase