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rs6922632

From SNPedia

Orientationplus
Stabilizedplus
Make rs6922632(A;A)
Make rs6922632(A;C)
Make rs6922632(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position24106865
is asnp
is mentioned by
dbSNPrs6922632
ebirs6922632
HLIrs6922632
Exacrs6922632
Varsomers6922632
Maprs6922632
PheGenIrs6922632
hapmaprs6922632
1000 genomesrs6922632
hgdprs6922632
ensemblrs6922632
gopubmedrs6922632
geneviewrs6922632
scholarrs6922632
googlers6922632
pharmgkbrs6922632
gwascentralrs6922632
openSNPrs6922632
23andMers6922632
23andMe allrs6922632
SNP Nexus

SNPshotrs6922632
SNPdbers6922632
MSV3drs6922632
GWAS Ctlgrs6922632
GMAF0.118
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21130836OA-icon.png]
Trait
Title Whole genome association scan for genetic polymorphisms influencing information processing speed
Risk Allele A
P-val 0.000004
Odds Ratio 0.1900 [0.11-0.27] unit increase