rs1358980
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1358980(C;C) |
Make rs1358980(C;T) |
Make rs1358980(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 43796814 |
Gene | LOC105375070 |
is a | snp |
is | mentioned by |
dbSNP | rs1358980 |
dbSNP (classic) | rs1358980 |
ClinGen | rs1358980 |
ebi | rs1358980 |
HLI | rs1358980 |
Exac | rs1358980 |
Gnomad | rs1358980 |
Varsome | rs1358980 |
LitVar | rs1358980 |
Map | rs1358980 |
PheGenI | rs1358980 |
Biobank | rs1358980 |
1000 genomes | rs1358980 |
hgdp | rs1358980 |
ensembl | rs1358980 |
geneview | rs1358980 |
scholar | rs1358980 |
rs1358980 | |
pharmgkb | rs1358980 |
gwascentral | rs1358980 |
openSNP | rs1358980 |
23andMe | rs1358980 |
SNPshot | rs1358980 |
SNPdbe | rs1358980 |
MSV3d | rs1358980 |
GWAS Ctlg | rs1358980 |
GMAF | 0.4389 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23754948![]() |
Trait | Sexual dimorphism in anthropometric traits |
Title | Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. |
Risk Allele | T |
P-val | 2E-11 |
Odds Ratio | NR NR |
[PMID 19308252] Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.