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rs776488

From SNPedia

Orientationplus
Stabilizedplus
Make rs776488(A;A)
Make rs776488(A;C)
Make rs776488(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position165034223
GeneLOC101929658
is asnp
is mentioned by
dbSNPrs776488
ebirs776488
HLIrs776488
Exacrs776488
Varsomers776488
Maprs776488
PheGenIrs776488
hapmaprs776488
1000 genomesrs776488
hgdprs776488
ensemblrs776488
gopubmedrs776488
geneviewrs776488
scholarrs776488
googlers776488
pharmgkbrs776488
gwascentralrs776488
openSNPrs776488
23andMers776488
23andMe allrs776488
SNP Nexus

SNPshotrs776488
SNPdbers776488
MSV3drs776488
GWAS Ctlgrs776488
GMAF0.1694
Max Magnitude
[PMID 20585627OA-icon.png] common trait being footedness
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20585627OA-icon.png]
Trait Common traits (Other)
Title Web-based, participant-driven studies yield novel genetic associations for common traits
Risk Allele
P-val 2E-7
Odds Ratio None None