rs11580946
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11580946(A;A) |
Make rs11580946(A;G) |
Make rs11580946(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 150578851 |
Gene | LOC107985203, MCL1 |
is a | snp |
is | mentioned by |
dbSNP | rs11580946 |
dbSNP (classic) | rs11580946 |
ClinGen | rs11580946 |
ebi | rs11580946 |
HLI | rs11580946 |
Exac | rs11580946 |
Gnomad | rs11580946 |
Varsome | rs11580946 |
LitVar | rs11580946 |
Map | rs11580946 |
PheGenI | rs11580946 |
Biobank | rs11580946 |
1000 genomes | rs11580946 |
hgdp | rs11580946 |
ensembl | rs11580946 |
geneview | rs11580946 |
scholar | rs11580946 |
rs11580946 | |
pharmgkb | rs11580946 |
gwascentral | rs11580946 |
openSNP | rs11580946 |
23andMe | rs11580946 |
SNPshot | rs11580946 |
SNPdbe | rs11580946 |
MSV3d | rs11580946 |
GWAS Ctlg | rs11580946 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.