rs114518130
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs114518130(A;A) |
Make rs114518130(A;G) |
Make rs114518130(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 57047087 |
Gene | IGFBP7 |
is a | snp |
is | mentioned by |
dbSNP | rs114518130 |
dbSNP (classic) | rs114518130 |
ClinGen | rs114518130 |
ebi | rs114518130 |
HLI | rs114518130 |
Exac | rs114518130 |
Gnomad | rs114518130 |
Varsome | rs114518130 |
LitVar | rs114518130 |
Map | rs114518130 |
PheGenI | rs114518130 |
Biobank | rs114518130 |
1000 genomes | rs114518130 |
hgdp | rs114518130 |
ensembl | rs114518130 |
geneview | rs114518130 |
scholar | rs114518130 |
rs114518130 | |
pharmgkb | rs114518130 |
gwascentral | rs114518130 |
openSNP | rs114518130 |
23andMe | rs114518130 |
SNPshot | rs114518130 |
SNPdbe | rs114518130 |
MSV3d | rs114518130 |
GWAS Ctlg | rs114518130 |
Max Magnitude | 0 |
[PMID 28763065] Genome-wide association analysis identifies common variants influencing infant brain volumes.