rs12635698
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12635698(C;C) |
Make rs12635698(C;T) |
Make rs12635698(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 16366982 |
Gene | OXNAD1, RFTN1 |
is a | snp |
is | mentioned by |
dbSNP | rs12635698 |
dbSNP (classic) | rs12635698 |
ClinGen | rs12635698 |
ebi | rs12635698 |
HLI | rs12635698 |
Exac | rs12635698 |
Gnomad | rs12635698 |
Varsome | rs12635698 |
LitVar | rs12635698 |
Map | rs12635698 |
PheGenI | rs12635698 |
Biobank | rs12635698 |
1000 genomes | rs12635698 |
hgdp | rs12635698 |
ensembl | rs12635698 |
geneview | rs12635698 |
scholar | rs12635698 |
rs12635698 | |
pharmgkb | rs12635698 |
gwascentral | rs12635698 |
openSNP | rs12635698 |
23andMe | rs12635698 |
SNPshot | rs12635698 |
SNPdbe | rs12635698 |
MSV3d | rs12635698 |
GWAS Ctlg | rs12635698 |
GMAF | 0.208 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19553259] |
Trait | Obesity (extreme) |
Title | Common BMI-associated variants confer risk of extreme obesity |
Risk Allele | C |
P-val | 0.000005 |
Odds Ratio | 1.41 [1.21-1.63] |
Occurs within the RFTN1 (Raftlin, lipid raft linker 1) gene