rs2052550
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs2052550(A;A) |
Make rs2052550(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 78977119 |
Gene | ARSB |
is a | snp |
is | mentioned by |
dbSNP | rs2052550 |
dbSNP (classic) | rs2052550 |
ClinGen | rs2052550 |
ebi | rs2052550 |
HLI | rs2052550 |
Exac | rs2052550 |
Gnomad | rs2052550 |
Varsome | rs2052550 |
LitVar | rs2052550 |
Map | rs2052550 |
PheGenI | rs2052550 |
Biobank | rs2052550 |
1000 genomes | rs2052550 |
hgdp | rs2052550 |
ensembl | rs2052550 |
geneview | rs2052550 |
scholar | rs2052550 |
rs2052550 | |
pharmgkb | rs2052550 |
gwascentral | rs2052550 |
openSNP | rs2052550 |
23andMe | rs2052550 |
SNPshot | rs2052550 |
SNPdbe | rs2052550 |
MSV3d | rs2052550 |
GWAS Ctlg | rs2052550 |
GMAF | 0.4885 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19084217] |
Trait | Serum markers of iron status |
Title | Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | NR NR |