Have questions? Visit https://www.reddit.com/r/SNPedia

rs7646881

From SNPedia

Orientationplus
Stabilizedplus
Make rs7646881(A;A)
Make rs7646881(A;C)
Make rs7646881(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position158735490
is asnp
is mentioned by
dbSNPrs7646881
ebirs7646881
HLIrs7646881
Exacrs7646881
Varsomers7646881
Maprs7646881
PheGenIrs7646881
hapmaprs7646881
1000 genomesrs7646881
hgdprs7646881
ensemblrs7646881
gopubmedrs7646881
geneviewrs7646881
scholarrs7646881
googlers7646881
pharmgkbrs7646881
gwascentralrs7646881
openSNPrs7646881
23andMers7646881
23andMe allrs7646881
SNP Nexus

SNPshotrs7646881
SNPdbers7646881
MSV3drs7646881
GWAS Ctlgrs7646881
GMAF0.1575
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23297363OA-icon.png]
Trait Tetralogy of Fallot
Title Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
Risk Allele A
P-val 2E-6
Odds Ratio 1.39 [1.224-1.581]