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rs2388896

From SNPedia

Orientationplus
Stabilizedplus
Make rs2388896(A;A)
Make rs2388896(A;G)
Make rs2388896(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position8912261
is asnp
is mentioned by
dbSNPrs2388896
ebirs2388896
HLIrs2388896
Exacrs2388896
Varsomers2388896
Maprs2388896
PheGenIrs2388896
hapmaprs2388896
1000 genomesrs2388896
hgdprs2388896
ensemblrs2388896
gopubmedrs2388896
geneviewrs2388896
scholarrs2388896
googlers2388896
pharmgkbrs2388896
gwascentralrs2388896
openSNPrs2388896
23andMers2388896
23andMe allrs2388896
SNP Nexus

SNPshotrs2388896
SNPdbers2388896
MSV3drs2388896
GWAS Ctlgrs2388896
GMAF0.32
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 9E-8
Odds Ratio 1.28 [1.15-1.43]