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rs7982677

From SNPedia

Orientationplus
Stabilizedplus
Make rs7982677(A;A)
Make rs7982677(A;C)
Make rs7982677(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position92336070
GeneGPC5
is asnp
is mentioned by
dbSNPrs7982677
ebirs7982677
HLIrs7982677
Exacrs7982677
Varsomers7982677
Maprs7982677
PheGenIrs7982677
hapmaprs7982677
1000 genomesrs7982677
hgdprs7982677
ensemblrs7982677
gopubmedrs7982677
geneviewrs7982677
scholarrs7982677
googlers7982677
pharmgkbrs7982677
gwascentralrs7982677
openSNPrs7982677
23andMers7982677
23andMe allrs7982677
SNP Nexus

SNPshotrs7982677
SNPdbers7982677
MSV3drs7982677
GWAS Ctlgrs7982677
GMAF0.2971
Max Magnitude
? (A;A) (A;C) (C;C) 28
Babies who are AC or AA at rs7982677 are about 1.3-1.7 times more likely to have tetralogy of Fallot (TOF) http://blog.23andme.com/23andme-research/snpwatch/snpwatch-common-genetic-factors-associated-with-blue-babies/
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 3E-9
Odds Ratio 1.29 [1.152-1.441]