rs9373124
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9373124(C;C) |
Make rs9373124(C;T) |
Make rs9373124(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 135102071 |
is a | snp |
is | mentioned by |
dbSNP | rs9373124 |
dbSNP (classic) | rs9373124 |
ClinGen | rs9373124 |
ebi | rs9373124 |
HLI | rs9373124 |
Exac | rs9373124 |
Gnomad | rs9373124 |
Varsome | rs9373124 |
LitVar | rs9373124 |
Map | rs9373124 |
PheGenI | rs9373124 |
Biobank | rs9373124 |
1000 genomes | rs9373124 |
hgdp | rs9373124 |
ensembl | rs9373124 |
geneview | rs9373124 |
scholar | rs9373124 |
rs9373124 | |
pharmgkb | rs9373124 |
gwascentral | rs9373124 |
openSNP | rs9373124 |
23andMe | rs9373124 |
SNPshot | rs9373124 |
SNPdbe | rs9373124 |
MSV3d | rs9373124 |
GWAS Ctlg | rs9373124 |
GMAF | 0.3356 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19862010] |
Trait | Other erythrocyte phenotypes |
Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
Risk Allele | C |
P-val | 7E-14 |
Odds Ratio | 0 [0.002-0.003] g/dl decrease |
GWAS snp | |
---|---|
PMID | [PMID 21738478] |
Trait | |
Title | Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. |
Risk Allele | T |
P-val | 1E-10 |
Odds Ratio | 0.0800 [0.06-0.10] unit increase |