rs1079572
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1079572(C;C) |
Make rs1079572(C;T) |
Make rs1079572(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 78153241 |
Gene | WWOX |
is a | snp |
is | mentioned by |
dbSNP | rs1079572 |
dbSNP (classic) | rs1079572 |
ClinGen | rs1079572 |
ebi | rs1079572 |
HLI | rs1079572 |
Exac | rs1079572 |
Gnomad | rs1079572 |
Varsome | rs1079572 |
LitVar | rs1079572 |
Map | rs1079572 |
PheGenI | rs1079572 |
Biobank | rs1079572 |
1000 genomes | rs1079572 |
hgdp | rs1079572 |
ensembl | rs1079572 |
geneview | rs1079572 |
scholar | rs1079572 |
rs1079572 | |
pharmgkb | rs1079572 |
gwascentral | rs1079572 |
openSNP | rs1079572 |
23andMe | rs1079572 |
SNPshot | rs1079572 |
SNPdbe | rs1079572 |
MSV3d | rs1079572 |
GWAS Ctlg | rs1079572 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24929828] |
Trait | Forced vital capacity |
Title | Genome-wide association analysis identifies six new loci associated with forced vital capacity. |
Risk Allele | G |
P-val | 1E-8 |
Odds Ratio | 16.26 [10.70-21.82] ml increase |