rs10514437
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10514437(A;A) |
Make rs10514437(A;G) |
Make rs10514437(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 78458963 |
Gene | WWOX |
is a | snp |
is | mentioned by |
dbSNP | rs10514437 |
dbSNP (classic) | rs10514437 |
ClinGen | rs10514437 |
ebi | rs10514437 |
HLI | rs10514437 |
Exac | rs10514437 |
Gnomad | rs10514437 |
Varsome | rs10514437 |
LitVar | rs10514437 |
Map | rs10514437 |
PheGenI | rs10514437 |
Biobank | rs10514437 |
1000 genomes | rs10514437 |
hgdp | rs10514437 |
ensembl | rs10514437 |
geneview | rs10514437 |
scholar | rs10514437 |
rs10514437 | |
pharmgkb | rs10514437 |
gwascentral | rs10514437 |
openSNP | rs10514437 |
23andMe | rs10514437 |
SNPshot | rs10514437 |
SNPdbe | rs10514437 |
MSV3d | rs10514437 |
GWAS Ctlg | rs10514437 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 28763065] Genome-wide association analysis identifies common variants influencing infant brain volumes.