rs79206939
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs79206939(A;A) |
Make rs79206939(A;G) |
Make rs79206939(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 53826140 |
Gene | FTO |
is a | snp |
is | mentioned by |
dbSNP | rs79206939 |
dbSNP (classic) | rs79206939 |
ClinGen | rs79206939 |
ebi | rs79206939 |
HLI | rs79206939 |
Exac | rs79206939 |
Gnomad | rs79206939 |
Varsome | rs79206939 |
LitVar | rs79206939 |
Map | rs79206939 |
PheGenI | rs79206939 |
Biobank | rs79206939 |
1000 genomes | rs79206939 |
hgdp | rs79206939 |
ensembl | rs79206939 |
geneview | rs79206939 |
scholar | rs79206939 |
rs79206939 | |
pharmgkb | rs79206939 |
gwascentral | rs79206939 |
openSNP | rs79206939 |
23andMe | rs79206939 |
SNPshot | rs79206939 |
SNPdbe | rs79206939 |
MSV3d | rs79206939 |
GWAS Ctlg | rs79206939 |
Max Magnitude | 0 |
[PMID 29463151] The role of FTO variants in the susceptibility of polycystic ovary syndrome and in vitro fertilization outcomes in Chinese women.