rs4466998
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4466998(A;A) |
Make rs4466998(A;C) |
Make rs4466998(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 65008822 |
Gene | CHURC1-FNTB, FNTB, MAX |
is a | snp |
is | mentioned by |
dbSNP | rs4466998 |
dbSNP (classic) | rs4466998 |
ClinGen | rs4466998 |
ebi | rs4466998 |
HLI | rs4466998 |
Exac | rs4466998 |
Gnomad | rs4466998 |
Varsome | rs4466998 |
LitVar | rs4466998 |
Map | rs4466998 |
PheGenI | rs4466998 |
Biobank | rs4466998 |
1000 genomes | rs4466998 |
hgdp | rs4466998 |
ensembl | rs4466998 |
geneview | rs4466998 |
scholar | rs4466998 |
rs4466998 | |
pharmgkb | rs4466998 |
gwascentral | rs4466998 |
openSNP | rs4466998 |
23andMe | rs4466998 |
SNPshot | rs4466998 |
SNPdbe | rs4466998 |
MSV3d | rs4466998 |
GWAS Ctlg | rs4466998 |
GMAF | 0.4417 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19862010] |
Trait | Mean corpuscular volume |
Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
Risk Allele | A |
P-val | 5E-8 |
Odds Ratio | 0 [0.001-0.003] fl increase |