rs7982677
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7982677(A;A) |
Make rs7982677(A;C) |
Make rs7982677(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 92336070 |
Gene | GPC5 |
is a | snp |
is | mentioned by |
dbSNP | rs7982677 |
dbSNP (classic) | rs7982677 |
ClinGen | rs7982677 |
ebi | rs7982677 |
HLI | rs7982677 |
Exac | rs7982677 |
Gnomad | rs7982677 |
Varsome | rs7982677 |
LitVar | rs7982677 |
Map | rs7982677 |
PheGenI | rs7982677 |
Biobank | rs7982677 |
1000 genomes | rs7982677 |
hgdp | rs7982677 |
ensembl | rs7982677 |
geneview | rs7982677 |
scholar | rs7982677 |
rs7982677 | |
pharmgkb | rs7982677 |
gwascentral | rs7982677 |
openSNP | rs7982677 |
23andMe | rs7982677 |
SNPshot | rs7982677 |
SNPdbe | rs7982677 |
MSV3d | rs7982677 |
GWAS Ctlg | rs7982677 |
GMAF | 0.2971 |
Max Magnitude | 0 |
? | (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 23297363] |
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] |