rs3091242
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3091242(C;C) |
Make rs3091242(C;T) |
Make rs3091242(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 25348294 |
Gene | TMEM50A |
is a | snp |
is | mentioned by |
dbSNP | rs3091242 |
dbSNP (classic) | rs3091242 |
ClinGen | rs3091242 |
ebi | rs3091242 |
HLI | rs3091242 |
Exac | rs3091242 |
Gnomad | rs3091242 |
Varsome | rs3091242 |
LitVar | rs3091242 |
Map | rs3091242 |
PheGenI | rs3091242 |
Biobank | rs3091242 |
1000 genomes | rs3091242 |
hgdp | rs3091242 |
ensembl | rs3091242 |
geneview | rs3091242 |
scholar | rs3091242 |
rs3091242 | |
pharmgkb | rs3091242 |
gwascentral | rs3091242 |
openSNP | rs3091242 |
23andMe | rs3091242 |
SNPshot | rs3091242 |
SNPdbe | rs3091242 |
MSV3d | rs3091242 |
GWAS Ctlg | rs3091242 |
GMAF | 0.376 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21700265![]() |
Trait | |
Title | Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. |
Risk Allele | |
P-val | 2E-13 |
Odds Ratio | 0.1000 [NR] unit decrease |