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rs6499100

From SNPedia

Orientationplus
Stabilizedplus
Make rs6499100(C;C)
Make rs6499100(C;T)
Make rs6499100(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position52797550
is asnp
is mentioned by
dbSNPrs6499100
ebirs6499100
HLIrs6499100
Exacrs6499100
Varsomers6499100
Maprs6499100
PheGenIrs6499100
hapmaprs6499100
1000 genomesrs6499100
hgdprs6499100
ensemblrs6499100
gopubmedrs6499100
geneviewrs6499100
scholarrs6499100
googlers6499100
pharmgkbrs6499100
gwascentralrs6499100
openSNPrs6499100
23andMers6499100
23andMe allrs6499100
SNP Nexus

SNPshotrs6499100
SNPdbers6499100
MSV3drs6499100
GWAS Ctlgrs6499100
GMAF0.4729
Max Magnitude
? (C;C) (C;T) (T;T) 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 1E-6
Odds Ratio 1.26 [1.14-1.4]